A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451732



Internal ID229905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:42067218..42095328hg38UCSC Ensembl
chr2:42294358..42322468hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3828111
hg1928111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16912224
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451732
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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