A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17392145



Internal ID22450015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:190124479..190129587hg38UCSC Ensembl
chr2:190989205..190994313hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg385109
hg195109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897206
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17392145
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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