A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427829



Internal ID22485699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155402741..155406986hg38UCSC Ensembl
chr3:155120530..155124775hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg384246
hg194246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896182
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427829
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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