A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195166



Internal ID20762206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2332828..2810839hg38UCSC Ensembl
chr11:2354058..2832069hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38478012
hg19478012
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445062
Supporting Variants
Samples
Known GenesCD81, CD81-AS1, KCNQ1, KCNQ1OT1, TRPM5, TSSC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195166
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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