A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516884



Internal ID15444177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:67353901..67436434hg38UCSC Ensembl
InnerchrX:66573743..66656276hg19UCSC Ensembl
InnerchrX:66490468..66573001hg18UCSC Ensembl
InnerchrX:66356764..66439297hg17UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3882534
hg1982534
hg1882534
hg1782534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv654682, nssv682508, nssv674865, nssv685681
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516884
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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