A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491536



Internal ID268772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:85727793..85732010hg38UCSC Ensembl
chr7:85357109..85361326hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg384218
hg194218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16999536
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491536
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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