A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141480



Internal ID340677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98026214..98028333hg38UCSC Ensembl
chr7:97655526..97657645hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg382120
hg192120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000462
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141480
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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