A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451138



Internal ID229324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:84892366..84895361hg38UCSC Ensembl
chr2:85119490..85122485hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg382996
hg192996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16917293
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451138
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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