A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527903



Internal ID15455196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:88759138..88933269hg38UCSC Ensembl
InnerchrX:88014139..88188270hg19UCSC Ensembl
InnerchrX:87900795..88074926hg18UCSC Ensembl
InnerchrX:87820284..87994415hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38174132
hg19174132
hg18174132
hg17174132
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv519n21
Supporting Variantsnssv704407
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527903
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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