A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434361



Internal ID213039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15782493..15782545hg38UCSC Ensembl
chr4:15784116..15784168hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16945250
Samples
Known GenesCD38
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434361
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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