A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018656



Internal ID19107873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:86801860..86844235hg38UCSC Ensembl
Innerchr8:87814088..87856463hg19UCSC Ensembl
Innerchr8:87883204..87925579hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3842376
hg1942376
hg1842376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689685
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)nsv1018656
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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