A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526895



Internal ID15454188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:141935576..141980130hg38UCSC Ensembl
InnerchrX:141023362..141067916hg19UCSC Ensembl
InnerchrX:140851028..140895582hg18UCSC Ensembl
InnerchrX:140748882..140793436hg17UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3844555
hg1944555
hg1844555
hg1744555
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703253
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526895
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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