A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020762



Internal ID19109980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16166714..16560861hg38UCSC Ensembl
Innerchr8:16024223..16418370hg19UCSC Ensembl
Innerchr8:16068594..16462741hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38394148
hg19394148
hg18394148
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3675959
Samples
Known GenesMSR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020762
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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