A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458027



Internal ID236060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75937424..75994818hg38UCSC Ensembl
chr6:76647141..76704535hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3857395
hg1957395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987313
Samples
Known GenesIMPG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458027
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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