A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065945



Internal ID19155164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78595683..78617066hg38UCSC Ensembl
Innerchr17:76591765..76613148hg19UCSC Ensembl
Innerchr17:74103360..74124743hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3821384
hg1921384
hg1821384
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567820
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)nsv1065945
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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