A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186268



Internal ID20753309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61988443..62108693hg38UCSC Ensembl
chr11:61755915..61876165hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38120251
hg19120251
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474406
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186268
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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