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nsv5458375

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:59

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 143 SVs from 23 studies. See in: genome view    
Submitted genomic82,898,047-82,898,105Question Mark
Overlapping variant regions from other studies: 143 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):83,819,200-83,819,258Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5458375Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr482,898,04782,898,105
nsv5458375RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr483,819,20083,819,258

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16951478deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16951478Submitted genomicNC_000004.12:g.828
98047_82898105del
GRCh38 (hg38)NC_000004.12Chr482,898,04782,898,105
nssv16951478RemappedPerfectNC_000004.11:g.838
19200_83819258del
GRCh37.p13First PassNC_000004.11Chr483,819,20083,819,258

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)
nssv16951478<0.00136404
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