A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521636



Internal ID15448929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:87985701..88150778hg38UCSC Ensembl
InnerchrX:87240701..87405779hg19UCSC Ensembl
InnerchrX:87127357..87292435hg18UCSC Ensembl
InnerchrX:87046846..87211924hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38165078
hg19165079
hg18165079
hg17165079
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698254
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521636
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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