A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105475



Internal ID20672515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95210689..95211184hg38UCSC Ensembl
chr3:94929533..94930028hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363366
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105475
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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