A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106599



Internal ID22015833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75033052..75033052hg38UCSC Ensembl
chr18:72745008..72745008hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628428
Samples
Known GenesZNF407
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106599
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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