A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437761



Internal ID216344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:6292795..6305154hg38UCSC Ensembl
chr2:6432927..6445286hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3812360
hg1912360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16909913
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437761
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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