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nsv6163015

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:287

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 197 SVs from 37 studies. See in: genome view    
Submitted genomic236,755,701-236,755,987Question Mark
Overlapping variant regions from other studies: 200 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):236,919,001-236,919,287Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6163015Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1236,755,701236,755,987
nsv6163015RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1236,919,001236,919,287

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17875951deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17875951Submitted genomicNC_000001.11:g.236
755701_236755987de
l
GRCh38 (hg38)NC_000001.11Chr1236,755,701236,755,987
nssv17875951RemappedPerfectNC_000001.10:g.236
919001_236919287de
l
GRCh37.p13First PassNC_000001.10Chr1236,919,001236,919,287

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)
nssv17875951<0.00112334
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