A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704550



Internal ID15441202
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528021
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704550
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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