A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17420792



Internal ID22478662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182008625..182013713hg38UCSC Ensembl
chr3:181726413..181731501hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg385089
hg195089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5903729
Supporting Variants
Samples
Known GenesLOC100996490
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17420792
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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