A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578914



Internal ID16019637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20553670..20638696hg38UCSC Ensembl
Innerchr19:20736476..20821502hg19UCSC Ensembl
Innerchr19:20528316..20613342hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3885027
hg1985027
hg1885027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv896517
Samples
Known GenesZNF626, ZNF737
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578914
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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