A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv898984



Internal ID15846254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36139901..36142743hg38UCSC Ensembl
Innerchr19:36630803..36633645hg19UCSC Ensembl
Innerchr19:41322643..41325485hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg382843
hg192843
hg182843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579424
Supporting Variants
Samples
Known GenesCAPNS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv898984
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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