A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18095380



Internal ID20662420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:161258294..161336333hg38UCSC Ensembl
chr3:160976082..161054121hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3878040
hg1978040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356465
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18095380
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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