A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv897469



Internal ID16191425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:28699611..28745959hg38UCSC Ensembl
Innerchr19:29190518..29236866hg19UCSC Ensembl
Innerchr19:33882358..33928706hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3846349
hg1946349
hg1846349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579239
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv897469
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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