A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv896537



Internal ID15843807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20618611..20802619hg38UCSC Ensembl
Innerchr19:20801417..20985425hg19UCSC Ensembl
Innerchr19:20593257..20777265hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38184009
hg19184009
hg18184009
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578921
Supporting Variants
Samples
Known GenesZNF626
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv896537
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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