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nsv5697537

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1
  • Description:Insertion of a Alu mobile element relative to the reference
  • Publication(s):Chuang et al. 2021

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 120 SVs from 23 studies. See in: genome view    
Submitted genomic41,799,481-41,799,481Question Mark
Overlapping variant regions from other studies: 114 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):42,303,413-42,303,413Question Mark
Overlapping variant regions from other studies: 8 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):368,520-368,520Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5697537Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1941,799,48141,799,481
nsv5697537RemappedPerfectGRCh37.p13Primary AssemblySecond PassNC_000019.9Chr1942,303,41342,303,413
nsv5697537RemappedPerfectGRCh37.p13PATCHESFirst PassNW_004775434.1Chr19|NW_0
04775434.1
368,520368,520

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17199858alu insertionSequencingOther
nssv17224618alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17199858Submitted genomicNC_000019.10:g.417
99481_41799482ins2
80
GRCh38 (hg38)NC_000019.10Chr1941,799,48141,799,481
nssv17224618Submitted genomicNC_000019.10:g.417
99481_41799482ins2
80
GRCh38 (hg38)NC_000019.10Chr1941,799,48141,799,481
nssv17199858RemappedPerfectNW_004775434.1:g.3
68520_368521ins280
GRCh37.p13First PassNW_004775434.1Chr19|NW_0
04775434.1
368,520368,520
nssv17224618RemappedPerfectNW_004775434.1:g.3
68520_368521ins280
GRCh37.p13First PassNW_004775434.1Chr19|NW_0
04775434.1
368,520368,520
nssv17199858RemappedPerfectNC_000019.9:g.4230
3413_42303414ins28
0
GRCh37.p13Second PassNC_000019.9Chr1942,303,41342,303,413
nssv17224618RemappedPerfectNC_000019.9:g.4230
3413_42303414ins28
0
GRCh37.p13Second PassNC_000019.9Chr1942,303,41342,303,413

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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