A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485534



Internal ID262923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154918027..154922348hg38UCSC Ensembl
chr7:154709737..154714058hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg384322
hg194322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17005322
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485534
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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