A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901160



Internal ID16195116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53369175..53426434hg38UCSC Ensembl
Innerchr19:53872428..53929687hg19UCSC Ensembl
Innerchr19:58564240..58621499hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3857260
hg1957260
hg1857260
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580081
Supporting Variants
Samples
Known GenesZNF525, ZNF765
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901160
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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