A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526997



Internal ID15454290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:118100969..118153229hg38UCSC Ensembl
InnerchrX:117234932..117287192hg19UCSC Ensembl
InnerchrX:117118960..117171220hg18UCSC Ensembl
InnerchrX:117016814..117069074hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3852261
hg1952261
hg1852261
hg1752261
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703372
Samples
Known GenesKLHL13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526997
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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