A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666620



Internal ID15403272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:113908725..113986808hg38UCSC Ensembl
InnerchrX:113152000..113230049hg19UCSC Ensembl
InnerchrX:113038265..113116314hg18UCSC Ensembl
InnerchrX:112957754..113035803hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3878084
hg1978050
hg1878050
hg1778050
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515718
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666620
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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