A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087546



Internal ID21996779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42423584..42423584hg38UCSC Ensembl
chr15:42715782..42715782hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608106
Samples
Known GenesZNF106
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087546
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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