A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696466



Internal ID15433118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:33916635..34003039hg38UCSC Ensembl
InnerchrX:33934752..34021156hg19UCSC Ensembl
InnerchrX:33844673..33931077hg18UCSC Ensembl
InnerchrX:33694409..33780813hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3886405
hg1986405
hg1886405
hg1786405
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520379
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696466
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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