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nsv5730937

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1
  • Description:Insertion of a SVA 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: 303 SVs from 41 studies. See in: genome view    
Submitted genomic17,461,374-17,461,374Question Mark
Overlapping variant regions from other studies: 303 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):17,461,483-17,461,483Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5730937Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr517,461,37417,461,374
nsv5730937RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr517,461,48317,461,483

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17235035sva insertionSequencingOther
nssv17248790sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17235035Submitted genomicNC_000005.10:g.174
61374_17461375ins1
240
GRCh38 (hg38)NC_000005.10Chr517,461,37417,461,374
nssv17248790Submitted genomicNC_000005.10:g.174
61374_17461375ins1
240
GRCh38 (hg38)NC_000005.10Chr517,461,37417,461,374
nssv17235035RemappedPerfectNC_000005.9:g.1746
1483_17461484ins12
40
GRCh37.p13First PassNC_000005.9Chr517,461,48317,461,483
nssv17248790RemappedPerfectNC_000005.9:g.1746
1483_17461484ins12
40
GRCh37.p13First PassNC_000005.9Chr517,461,48317,461,483

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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