A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464678



Internal ID242550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73518899..73519825hg38UCSC Ensembl
chr6:74228622..74229548hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38927
hg19927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16984166
Samples
Known GenesEEF1A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464678
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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