A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18095221



Internal ID20662261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123030429..123034169hg38UCSC Ensembl
chr3:122749276..122753016hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg383741
hg193741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363337
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18095221
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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