A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406004



Internal ID22463874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:67626768..67631402hg38UCSC Ensembl
chr2:67853900..67858534hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg384635
hg194635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869382
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406004
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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