A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899918



Internal ID15847188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43907391..43985872hg38UCSC Ensembl
Innerchr19:44411543..44490024hg19UCSC Ensembl
Innerchr19:49103383..49181864hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3878482
hg1978482
hg1878482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579854
Supporting Variants
Samples
Known GenesZNF155, ZNF221, ZNF45
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899918
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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