A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061771



Internal ID18804302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20646773..20782613hg38UCSC Ensembl
Innerchr19:20829579..20965419hg19UCSC Ensembl
Innerchr19:20621419..20757259hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38135841
hg19135841
hg18135841
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3467n100
Supporting Variantsnssv3570552, nssv3724302
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)nsv1061771
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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