A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694379



Internal ID15431031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:87497529..87607426hg38UCSC Ensembl
InnerchrX:86752532..86862429hg19UCSC Ensembl
InnerchrX:86639188..86749085hg18UCSC Ensembl
InnerchrX:86558677..86668574hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38109898
hg19109898
hg18109898
hg17109898
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)nssv694379
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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