A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523912



Internal ID15451205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:27146388..27417191hg38UCSC Ensembl
InnerchrX:27164505..27435308hg19UCSC Ensembl
InnerchrX:27074426..27345229hg18UCSC Ensembl
InnerchrX:26924162..27194965hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38270804
hg19270804
hg18270804
hg17270804
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699755
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523912
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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