A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092870



Internal ID20659910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:115453780..115454271hg38UCSC Ensembl
chr3:115172627..115173118hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38492
hg19492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357859
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092870
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00059


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