A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525963



Internal ID15453256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:4361359..4388553hg38UCSC Ensembl
InnerchrX:4279400..4306594hg19UCSC Ensembl
InnerchrX:4289400..4316594hg18UCSC Ensembl
InnerchrX:4139136..4166330hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3827195
hg1927195
hg1827195
hg1727195
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702175
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525963
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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