A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458763



Internal ID236784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75000811..75017342hg38UCSC Ensembl
chr6:75710527..75727058hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3816532
hg1916532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985588
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458763
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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