A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476662



Internal ID254267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:83881075..83881666hg38UCSC Ensembl
chr7:83510391..83510982hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16998935
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476662
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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