A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488737



Internal ID266036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43634190..43634293hg38UCSC Ensembl
chr7:43673789..43673892hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16997294
Samples
Known GenesCOA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488737
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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