A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434709



Internal ID213377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:18955398..18961195hg38UCSC Ensembl
chr2:19136676..19142473hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg385798
hg195798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16911127
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434709
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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