A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065764



Internal ID19154983
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 StatusM
Merged Variants
Supporting Variantsnssv3560084
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)nsv1065764
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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