A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068340



Internal ID20635380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45492694..45499024hg38UCSC Ensembl
chr20:44121334..44127664hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg386331
hg196331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552382
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068340
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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