A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv896603



Internal ID16190559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:21767535..21825427hg38UCSC Ensembl
Innerchr19:21950337..22008229hg19UCSC Ensembl
Innerchr19:21742177..21800069hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3857893
hg1957893
hg1857893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578971
Supporting Variants
Samples
Known GenesZNF100, ZNF43
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv896603
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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