A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061596



Internal ID18804127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20643872..20803497hg38UCSC Ensembl
Innerchr19:20826678..20986303hg19UCSC Ensembl
Innerchr19:20618518..20778143hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38159626
hg19159626
hg18159626
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3467n100
Supporting Variantsnssv3570548, nssv3570547
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)nsv1061596
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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