A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694092



Internal ID15084058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:27692376..27821455hg38UCSC Ensembl
InnerchrX:27710493..27839572hg19UCSC Ensembl
InnerchrX:27620414..27749493hg18UCSC Ensembl
InnerchrX:27470150..27599229hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38129080
hg19129080
hg18129080
hg17129080
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521729
Supporting Variants
Samples
Known GenesDCAF8L2, MAGEB10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694092
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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