A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17396969



Internal ID22454839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16305204..16305282hg38UCSC Ensembl
chr2:16486472..16486550hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871529
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17396969
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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