A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705606



Internal ID15442258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:88759138..88997898hg38UCSC Ensembl
InnerchrX:88014139..88252899hg19UCSC Ensembl
InnerchrX:87900795..88139555hg18UCSC Ensembl
InnerchrX:87820284..88059044hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38238761
hg19238761
hg18238761
hg17238761
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528918
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705606
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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