A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437936



Internal ID216511
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 StatusM
Merged Variants
Supporting Variantsnssv16914744
Samples
Known GenesLRRTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437936
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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