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nsv5717573

  • 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: 301 SVs from 26 studies. See in: genome view    
Submitted genomic44,030,355-44,030,355Question Mark
Overlapping variant regions from other studies: 301 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):45,450,236-45,450,236Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5717573Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2144,030,35544,030,355
nsv5717573RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2145,450,23645,450,236

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17237662sva insertionSequencingOther
nssv17253141sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17237662Submitted genomicNC_000021.9:g.4403
0355_44030356ins12
40
GRCh38 (hg38)NC_000021.9Chr2144,030,35544,030,355
nssv17253141Submitted genomicNC_000021.9:g.4403
0355_44030356ins20
4
GRCh38 (hg38)NC_000021.9Chr2144,030,35544,030,355
nssv17237662RemappedPerfectNC_000021.8:g.4545
0236_45450237ins12
40
GRCh37.p13First PassNC_000021.8Chr2145,450,23645,450,236
nssv17253141RemappedPerfectNC_000021.8:g.4545
0236_45450237ins20
4
GRCh37.p13First PassNC_000021.8Chr2145,450,23645,450,236

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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