A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5537872



Internal ID313065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9725731..9725749hg38UCSC Ensembl
chr3:9767415..9767433hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16930853
Samples
Known GenesCPNE9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5537872
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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