A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464906



Internal ID242777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14734015..14734379hg38UCSC Ensembl
chr6:14734246..14734610hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979149
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464906
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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