A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436793



Internal ID215400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:4521601..4531618hg38UCSC Ensembl
chr2:4569191..4579208hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3810018
hg1910018
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16909598
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436793
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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