A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3724978



Internal ID19023259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52428519..52508733hg38UCSC Ensembl
Innerchr17:50505879..50586093hg19UCSC Ensembl
Innerchr17:47860878..47941092hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3880215
hg1980215
hg1880215
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060938
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)nssv3724978
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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