A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682761



Internal ID15072727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:43170260..43390953hg38UCSC Ensembl
InnerchrX:43029509..43250202hg19UCSC Ensembl
InnerchrX:42914453..43135146hg18UCSC Ensembl
InnerchrX:42785763..43006456hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38220694
hg19220694
hg18220694
hg17220694
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517077
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682761
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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