A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5462935



Internal ID240854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56894919..56895948hg38UCSC Ensembl
chr4:57761085..57762114hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381030
hg191030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16951138
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5462935
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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