A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17398447



Internal ID22456317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173741643..173744337hg38UCSC Ensembl
chr2:174606371..174609065hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg382695
hg192695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905579
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17398447
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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