A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065615



Internal ID18808146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20646773..20814219hg38UCSC Ensembl
Innerchr19:20829579..20997025hg19UCSC Ensembl
Innerchr19:20621419..20788865hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38167447
hg19167447
hg18167447
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3467n100
Supporting Variantsnssv3724318
Samples
Known GenesZNF626
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065615
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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