A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015812



Internal ID19105030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:46634461..46831628hg38UCSC Ensembl
Innerchr8:47546083..47743250hg19UCSC Ensembl
Innerchr8:47665248..47862415hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg38197168
hg19197168
hg18197168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3687450
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)nsv1015812
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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