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nsv5458304

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:568,858

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2070 SVs from 81 studies. See in: genome view    
Submitted genomic87,152,087-87,720,944Question Mark
Overlapping variant regions from other studies: 2070 SVs from 81 studies. See in: genome view    
Remapped(Score: Perfect):88,073,239-88,642,096Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5458304Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr487,152,08787,720,944
nsv5458304RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr488,073,23988,642,096

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16953722deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16953722Submitted genomicNC_000004.12:g.871
52087_87720944del
GRCh38 (hg38)NC_000004.12Chr487,152,08787,720,944
nssv16953722RemappedPerfectNC_000004.11:g.880
73239_88642096del
GRCh37.p13First PassNC_000004.11Chr488,073,23988,642,096

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)
nssv16953722<0.00126404
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