A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564766



Internal ID18516361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12454604..12567252hg38UCSC Ensembl
Innerchr19:12565418..12678066hg19UCSC Ensembl
Innerchr19:12426418..12539066hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38112649
hg19112649
hg18112649
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065773
Supporting Variants
Samples
Known GenesZNF564, ZNF709
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564766
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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