A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17420293



Internal ID22478163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16309479..16309571hg38UCSC Ensembl
chr3:16350986..16351078hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5892636
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17420293
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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