A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105197



Internal ID20672237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77731338..77733498hg38UCSC Ensembl
chr3:77780489..77782649hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg382161
hg192161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366223
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105197
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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