A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv896171



Internal ID16190127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20396431..20588017hg38UCSC Ensembl
Innerchr19:20576399..20770823hg19UCSC Ensembl
Innerchr19:20368239..20562663hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38191587
hg19194425
hg18194425
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578817
Supporting Variants
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF737, ZNF826P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv896171
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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