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nsv5720636

  • 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: 147 SVs from 32 studies. See in: genome view    
Submitted genomic68,035,703-68,035,703Question Mark
Overlapping variant regions from other studies: 147 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):68,069,606-68,069,606Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5720636Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1668,035,70368,035,703
nsv5720636RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1668,069,60668,069,606

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17245896sva insertionSequencingOther
nssv17245902sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17245896Submitted genomicNC_000016.10:g.680
35703_68035704ins1
240
GRCh38 (hg38)NC_000016.10Chr1668,035,70368,035,703
nssv17245902Submitted genomicNC_000016.10:g.680
35703_68035704ins1
240
GRCh38 (hg38)NC_000016.10Chr1668,035,70368,035,703
nssv17245896RemappedPerfectNC_000016.9:g.6806
9606_68069607ins12
40
GRCh37.p13First PassNC_000016.9Chr1668,069,60668,069,606
nssv17245902RemappedPerfectNC_000016.9:g.6806
9606_68069607ins12
40
GRCh37.p13First PassNC_000016.9Chr1668,069,60668,069,606

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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