A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406532



Internal ID22464402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17832791..17833722hg38UCSC Ensembl
chr2:18014058..18014989hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg38932
hg19932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885072
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406532
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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