A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092365



Internal ID20659406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101128492..101128936hg38UCSC Ensembl
chr3:100847336..100847780hg19UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368228
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092365
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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