A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662117



Internal ID15052083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:12768002..12789612hg38UCSC Ensembl
InnerchrX:12786121..12807731hg19UCSC Ensembl
InnerchrX:12696042..12717652hg18UCSC Ensembl
InnerchrX:12545778..12567388hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3821611
hg1921611
hg1821611
hg1721611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520250
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662117
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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