A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528021



Internal ID15455314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35449939..35550496hg38UCSC Ensembl
Innerchr3:35491431..35591988hg19UCSC Ensembl
Innerchr3:35466435..35566992hg18UCSC Ensembl
Innerchr3:35466435..35566992hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38100558
hg19100558
hg18100558
hg17100558
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704550
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528021
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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