A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16927435



Internal ID18999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:181699618..181727618hg38UCSC Ensembl
chr2:182564345..182592345hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg3828001
hg1928001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5444300
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16927435
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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