A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578913



Internal ID16019636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20547679..20673648hg38UCSC Ensembl
Innerchr19:20730485..20856454hg19UCSC Ensembl
Innerchr19:20522325..20648294hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38125970
hg19125970
hg18125970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv896516
Samples
Known GenesZNF626, ZNF737
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578913
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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