A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460274



Internal ID238264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138697640..138707591hg38UCSC Ensembl
chr4:139618794..139628745hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg389952
hg199952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16957474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460274
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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