A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5445333



Internal ID223686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:76644540..76760874hg38UCSC Ensembl
chr2:76871666..76988000hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38116335
hg19116335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16915565
Samples
Known GenesLRRTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5445333
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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