A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16915398



Internal ID11005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100218759..100224874hg38UCSC Ensembl
chr2:100835221..100841336hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg386116
hg196116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435819
Supporting Variants
Samples
Known GenesLINC01104
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16915398
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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