A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16915216



Internal ID10887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:86687950..86701116hg38UCSC Ensembl
chr2:86915073..86928239hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3813167
hg1913167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139959
Supporting Variants
Samples
Known GenesRNF103-CHMP3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16915216
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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