A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523793



Internal ID15451086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:140572317..140574753hg38UCSC Ensembl
InnerchrX:139654482..139656918hg19UCSC Ensembl
InnerchrX:139482148..139484584hg18UCSC Ensembl
InnerchrX:139380002..139382438hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg382437
hg192437
hg182437
hg172437
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699621
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523793
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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