A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17396684



Internal ID22454554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21932658..21932997hg38UCSC Ensembl
chr2:22155530..22155869hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869204
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17396684
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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