A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578819



Internal ID16019542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20396431..20638696hg38UCSC Ensembl
Innerchr19:20576399..20821502hg19UCSC Ensembl
Innerchr19:20368239..20613342hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38242266
hg19245104
hg18245104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6304n54
Supporting Variantsnssv896175, nssv896176
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)nsv578819
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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