A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17398245



Internal ID22456115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126556879..126556930hg38UCSC Ensembl
chr3:126275722..126275773hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5890794
Supporting Variants
Samples
Known GenesC3orf22
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17398245
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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