A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16914744



Internal ID10578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:76753988..76754048hg38UCSC Ensembl
chr2:76981114..76981174hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437936
Supporting Variants
Samples
Known GenesLRRTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16914744
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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