A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560084



Internal ID18858365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:2784673..2908757hg38UCSC Ensembl
Innerchr17:2687967..2812051hg19UCSC Ensembl
Innerchr17:2634717..2758801hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38124085
hg19124085
hg18124085
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065764
Supporting Variants
Samples
Known GenesRAP1GAP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3560084
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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