A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460060



Internal ID238059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75926351..75930544hg38UCSC Ensembl
chr6:76636068..76640261hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg384194
hg194194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987311
Samples
Known GenesIMPG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460060
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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