A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528200



Internal ID15455493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:63004343..63060649hg38UCSC Ensembl
InnerchrX:62223813..62280119hg19UCSC Ensembl
InnerchrX:62140538..62196844hg18UCSC Ensembl
InnerchrX:62006834..62063140hg17UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3856307
hg1956307
hg1856307
hg1756307
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704760
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528200
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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