A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527156



Internal ID15454449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:94096802..94174579hg38UCSC Ensembl
InnerchrX:93351801..93429578hg19UCSC Ensembl
InnerchrX:93238457..93316234hg18UCSC Ensembl
InnerchrX:93157946..93235723hg17UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg3877778
hg1977778
hg1877778
hg1777778
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703548
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527156
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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