A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687425



Internal ID15424077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:87412105..87597220hg38UCSC Ensembl
InnerchrX:86667108..86852223hg19UCSC Ensembl
InnerchrX:86553764..86738879hg18UCSC Ensembl
InnerchrX:86473253..86658368hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38185116
hg19185116
hg18185116
hg17185116
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)nssv687425
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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