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nsv4524999

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:200

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 36 SVs from 10 studies. See in: genome view    
Remapped(Score: Perfect):98,880,601-98,880,800Question Mark
Overlapping variant regions from other studies: 35 SVs from 10 studies. See in: genome view    
Submitted genomic98,478,224-98,478,423Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4524999RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr798,880,60198,880,800
nsv4524999Submitted genomicGRCh37.p13Primary AssemblyNC_000007.13Chr798,478,22498,478,423

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15981890duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15981890RemappedPerfectNC_000007.14:g.988
80601_98880800dup
GRCh38.p12First PassNC_000007.14Chr798,880,60198,880,800
nssv15981890Submitted genomicNC_000007.13:g.984
78224_98478423dup
GRCh37.p13NC_000007.13Chr798,478,22498,478,423

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)
nssv159818904.6e-005121690
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