A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065008



Internal ID19154227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:57898770..57921861hg38UCSC Ensembl
Innerchr20:56473826..56496917hg19UCSC Ensembl
Innerchr20:55907232..55930323hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3823092
hg1923092
hg1823092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4334n100
Supporting Variantsnssv3584241
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)nsv1065008
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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