A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv896175



Internal ID15843445
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 StatusS
Merged Variantsnsv578819
Supporting Variants
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)nssv896175
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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