A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527045



Internal ID15454338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:43543475..43633941hg38UCSC Ensembl
InnerchrX:43402723..43493189hg19UCSC Ensembl
InnerchrX:43287667..43378133hg18UCSC Ensembl
InnerchrX:43158977..43249443hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3890467
hg1990467
hg1890467
hg1790467
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703421
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527045
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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