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nsv5440068

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,543

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 160 SVs from 29 studies. See in: genome view    
Submitted genomic182,577,168-182,578,710Question Mark
Overlapping variant regions from other studies: 162 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):182,546,303-182,547,845Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5440068Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1182,577,168182,578,710
nsv5440068RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1182,546,303182,547,845

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16892809deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16892809Submitted genomicNC_000001.11:g.182
577168_182578710de
l
GRCh38 (hg38)NC_000001.11Chr1182,577,168182,578,710
nssv16892809RemappedPerfectNC_000001.10:g.182
546303_182547845de
l
GRCh37.p13First PassNC_000001.10Chr1182,546,303182,547,845

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)
nssv16892809<0.00116404
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