A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698113



Internal ID15434765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:87511338..87558353hg38UCSC Ensembl
InnerchrX:86766341..86813356hg19UCSC Ensembl
InnerchrX:86652997..86700012hg18UCSC Ensembl
InnerchrX:86572486..86619501hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3847016
hg1947016
hg1847016
hg1747016
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)nssv698113
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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