A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094973



Internal ID20662013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137022432..137024596hg38UCSC Ensembl
chr3:136741274..136743438hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg382165
hg192165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374410
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094973
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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