A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464764



Internal ID242635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13461010..13471416hg38UCSC Ensembl
chr6:13461242..13471648hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3810407
hg1910407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979674
Samples
Known GenesGFOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464764
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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