A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526569



Internal ID15453862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195317558..195402766hg38UCSC Ensembl
Innerchr3:195038287..195123495hg19UCSC Ensembl
Innerchr3:196519576..196604784hg18UCSC Ensembl
Innerchr3:196519584..196604792hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3885209
hg1985209
hg1885209
hg1785209
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702885
Samples
Known GenesACAP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526569
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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