A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437084



Internal ID215683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215037824..215039758hg38UCSC Ensembl
chr2:215902548..215904482hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg381935
hg191935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16928162
Samples
Known GenesABCA12
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437084
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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