A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067256



Internal ID18809787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20646773..20797495hg38UCSC Ensembl
Innerchr19:20829579..20980301hg19UCSC Ensembl
Innerchr19:20621419..20772141hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38150723
hg19150723
hg18150723
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3467n100
Supporting Variantsnssv3570557, nssv3724310, nssv3724309
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)nsv1067256
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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