A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697315



Internal ID15433967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:87511338..87773848hg38UCSC Ensembl
InnerchrX:86766341..87028848hg19UCSC Ensembl
InnerchrX:86652997..86915504hg18UCSC Ensembl
InnerchrX:86572486..86834993hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38262511
hg19262508
hg18262508
hg17262508
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520266
Supporting Variants
Samples
Known GenesKLHL4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697315
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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