A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564696



Internal ID18516291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11802103..11950569hg38UCSC Ensembl
Innerchr19:11912918..12061384hg19UCSC Ensembl
Innerchr19:11773918..11922384hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38148467
hg19148467
hg18148467
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063853
Supporting Variants
Samples
Known GenesZNF439, ZNF440, ZNF491, ZNF69, ZNF700
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564696
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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