A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525822



Internal ID15453115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:4576615..4947777hg38UCSC Ensembl
InnerchrX:4494656..4865818hg19UCSC Ensembl
InnerchrX:4504656..4875818hg18UCSC Ensembl
InnerchrX:4354392..4725554hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg38371163
hg19371163
hg18371163
hg17371163
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702009
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525822
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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