A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521321



Internal ID15448614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:93449287..93533554hg38UCSC Ensembl
InnerchrX:92704286..92788553hg19UCSC Ensembl
InnerchrX:92590942..92675209hg18UCSC Ensembl
InnerchrX:92510431..92594698hg17UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg3884268
hg1984268
hg1884268
hg1784268
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697928
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521321
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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