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nsv5402078

  • 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: 121 SVs from 17 studies. See in: genome view    
Submitted genomic201,939,908-201,939,959Question Mark
Overlapping variant regions from other studies: 121 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):201,909,036-201,909,087Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5402078Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1201,939,908201,939,959
nsv5402078RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1201,909,036201,909,087

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16894697alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16894697Submitted genomicNC_000001.11:g.201
939908_201939959in
s276
GRCh38 (hg38)NC_000001.11Chr1201,939,908201,939,959
nssv16894697RemappedPerfectNC_000001.10:g.201
909036_201909087in
s276
GRCh37.p13First PassNC_000001.10Chr1201,909,036201,909,087

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)
nssv16894697<0.00126404
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