A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661263



Internal ID15397915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:114455270..114539177hg38UCSC Ensembl
InnerchrX:113689723..113773630hg19UCSC Ensembl
InnerchrX:113595979..113679886hg18UCSC Ensembl
InnerchrX:113512703..113596610hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3883908
hg1983908
hg1883908
hg1783908
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520153
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661263
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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