A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519858



Internal ID15447151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:81897849..82021231hg38UCSC Ensembl
InnerchrX:81153348..81276680hg19UCSC Ensembl
InnerchrX:81040004..81163336hg18UCSC Ensembl
InnerchrX:80959493..81082825hg17UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38123383
hg19123333
hg18123333
hg17123333
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697089
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519858
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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