A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487559



Internal ID264892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:68023424..68024128hg38UCSC Ensembl
chr7:67488411..67489115hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16997692
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487559
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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