A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673360



Internal ID15063326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:66486237..66797185hg38UCSC Ensembl
InnerchrX:65706079..66017027hg19UCSC Ensembl
InnerchrX:65622804..65933752hg18UCSC Ensembl
InnerchrX:65489100..65800048hg17UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38310949
hg19310949
hg18310949
hg17310949
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520630
Supporting Variants
Samples
Known GenesEDA2R
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673360
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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