A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020323



Internal ID19109542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:60988853..61028825hg38UCSC Ensembl
Innerchr8:61901412..61941384hg19UCSC Ensembl
Innerchr8:62063966..62103938hg18UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg3839973
hg1939973
hg1839973
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689468
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)nsv1020323
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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