A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899919



Internal ID15847189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44347982..44426176hg38UCSC Ensembl
Innerchr19:44852134..44930348hg19UCSC Ensembl
Innerchr19:49543974..49622188hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3878195
hg1978215
hg1878215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579855
Supporting Variants
Samples
Known GenesZNF112, ZNF285
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899919
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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