A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661376



Internal ID15398028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:87430890..87607718hg38UCSC Ensembl
InnerchrX:86685893..86862721hg19UCSC Ensembl
InnerchrX:86572549..86749377hg18UCSC Ensembl
InnerchrX:86492038..86668866hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38176829
hg19176829
hg18176829
hg17176829
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520176
Supporting Variants
Samples
Known GenesKLHL4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661376
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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