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nsv5561701

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 90 SVs from 19 studies. See in: genome view    
Submitted genomic34,084,759-34,084,810Question Mark
Overlapping variant regions from other studies: 90 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):34,480,748-34,480,799Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5561701Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2234,084,75934,084,810
nsv5561701RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2234,480,74834,480,799

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17728636line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17728636Submitted genomicNC_000022.11:g.340
84759_34084810ins7
0
GRCh38 (hg38)NC_000022.11Chr2234,084,75934,084,810
nssv17728636RemappedPerfectNC_000022.10:g.344
80748_34480799ins7
0
GRCh37.p13First PassNC_000022.10Chr2234,480,74834,480,799

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17728636<0.00126404
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