A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17398303



Internal ID22456173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191547758..191550213hg38UCSC Ensembl
chr2:192412484..192414939hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg382456
hg192456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906231
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17398303
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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