A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv897023



Internal ID16190979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24431519..24444706hg38UCSC Ensembl
Innerchr19:24614321..24627508hg19UCSC Ensembl
Innerchr19:24406161..24419348hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg3813188
hg1913188
hg1813188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579115
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)nssv897023
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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