A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526411



Internal ID15107018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:45810991..46476384hg38UCSC Ensembl
InnerchrX:45670405..46335819hg19UCSC Ensembl
InnerchrX:45555349..46220763hg18UCSC Ensembl
InnerchrX:45426659..46092073hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38665394
hg19665415
hg18665415
hg17665415
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702711
Samples
Known GenesKRBOX4, MIR5689
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526411
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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