A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv896601



Internal ID15843871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:21614141..21836895hg38UCSC Ensembl
Innerchr19:21796943..22019697hg19UCSC Ensembl
Innerchr19:21588783..21811537hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38222755
hg19222755
hg18222755
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578969
Supporting Variants
Samples
Known GenesLOC641367, ZNF100, ZNF43
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv896601
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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