A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520612



Internal ID15447905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:27230559..27337576hg38UCSC Ensembl
InnerchrX:27248676..27355693hg19UCSC Ensembl
InnerchrX:27158597..27265614hg18UCSC Ensembl
InnerchrX:27008333..27115350hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38107018
hg19107018
hg18107018
hg17107018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697518
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520612
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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