A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484791



Internal ID262197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90441521..90477958hg38UCSC Ensembl
chr7:90070835..90107272hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3836438
hg1936438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17002082
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484791
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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