A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402150



Internal ID22460020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:183174650..183176824hg38UCSC Ensembl
chr2:184039378..184041552hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg382175
hg192175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5904790
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402150
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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