A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16918876



Internal ID13358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:136019877..136031119hg38UCSC Ensembl
chr2:136777447..136788689hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg3811243
hg1911243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442317
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16918876
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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