A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062982



Internal ID19152201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67272716..67320089hg38UCSC Ensembl
Innerchr17:65268832..65316205hg19UCSC Ensembl
Innerchr17:62699294..62746667hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3847374
hg1947374
hg1847374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567745
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062982
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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