A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578970



Internal ID16019693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:21723853..21791127hg38UCSC Ensembl
Innerchr19:21906655..21973929hg19UCSC Ensembl
Innerchr19:21698495..21765769hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3867275
hg1967275
hg1867275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv896602
Samples
Known GenesLOC641367, ZNF100
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578970
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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