A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491696



Internal ID268928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74433438..74433601hg38UCSC Ensembl
chr7:73847768..73847931hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000980
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491696
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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