A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093289



Internal ID20660329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137595763..137600937hg38UCSC Ensembl
chr3:137314605..137319779hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg385175
hg195175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359279
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093289
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0004


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