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nsv5525955

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:297

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 120 SVs from 20 studies. See in: genome view    
Submitted genomic62,663,962-62,664,258Question Mark
Overlapping variant regions from other studies: 120 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):60,741,323-60,741,619Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5525955Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1762,663,96262,664,258
nsv5525955RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1760,741,32360,741,619

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17713947deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17713947Submitted genomicNC_000017.11:g.626
63962_62664258del
GRCh38 (hg38)NC_000017.11Chr1762,663,96262,664,258
nssv17713947RemappedPerfectNC_000017.10:g.607
41323_60741619del
GRCh37.p13First PassNC_000017.10Chr1760,741,32360,741,619

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)
nssv17713947<0.00126404
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