A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524582



Internal ID15105189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:114067803..114619628hg38UCSC Ensembl
InnerchrX:113310992..113854086hg19UCSC Ensembl
InnerchrX:113197257..113760342hg18UCSC Ensembl
InnerchrX:113116746..113677066hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38551826
hg19543095
hg18563086
hg17560321
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv524n21
Supporting Variantsnssv700539
Samples
Known GenesHTR2C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524582
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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