A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567762



Internal ID18866043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:70439183..70639700hg38UCSC Ensembl
Innerchr17:68435324..68635841hg19UCSC Ensembl
Innerchr17:65946919..66147436hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38200518
hg19200518
hg18200518
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063095
Supporting Variants
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)nssv3567762
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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