A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578818



Internal ID16366227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20396431..20626370hg38UCSC Ensembl
Innerchr19:20576399..20809176hg19UCSC Ensembl
Innerchr19:20368239..20601016hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38229940
hg19232778
hg18232778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6304n54
Supporting Variantsnssv896174
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF626, ZNF737, ZNF826P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578818
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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