A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465738



Internal ID243594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9494456..9494765hg38UCSC Ensembl
chr6:9494689..9494998hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979473
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465738
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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