A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16915547



Internal ID11099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:76423696..77536175hg38UCSC Ensembl
chr2:76650822..77763301hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg381112480
hg191112480
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442937
Supporting Variants
Samples
Known GenesLRRTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16915547
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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