A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436412



Internal ID215029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:136237504..136239046hg38UCSC Ensembl
chr2:136995074..136996616hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg381543
hg191543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16919702
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436412
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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