A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523656



Internal ID15450949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:126178122..126251354hg38UCSC Ensembl
InnerchrX:125312105..125385337hg19UCSC Ensembl
InnerchrX:125139786..125213018hg18UCSC Ensembl
InnerchrX:125037640..125110872hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3873233
hg1973233
hg1873233
hg1773233
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699457
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523656
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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