A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015512



Internal ID19104729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15784704..15956559hg38UCSC Ensembl
Innerchr8:15642213..15814068hg19UCSC Ensembl
Innerchr8:15686584..15858439hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38171856
hg19171856
hg18171856
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3675904
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)nsv1015512
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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