A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096608



Internal ID22005841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:43457056..43457056hg38UCSC Ensembl
chr13:44031192..44031192hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597575
Samples
Known GenesENOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096608
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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