A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578802



Internal ID16366211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19980893..20553670hg38UCSC Ensembl
Innerchr19:20091702..20736476hg19UCSC Ensembl
Innerchr19:19952702..20528316hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38572778
hg19644775
hg18575615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6303n54
Supporting Variantsnssv896159
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF486, ZNF682, ZNF737, ZNF826P, ZNF90
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578802
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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