A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17397689



Internal ID22455559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:18854471..18854522hg38UCSC Ensembl
chr2:19035737..19035788hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882387
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17397689
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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