A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679243



Internal ID15415895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:69916258..69970295hg38UCSC Ensembl
InnerchrX:69136101..69190145hg19UCSC Ensembl
InnerchrX:69052826..69106870hg18UCSC Ensembl
InnerchrX:68919122..68973166hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3854038
hg1954045
hg1854045
hg1754045
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520990
Supporting Variants
Samples
Known GenesEDA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679243
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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