A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764170



Internal ID20540030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44750637..44750637hg38UCSC Ensembl
chr20:43379278..43379278hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292835
Samples
Known GenesKCNK15
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764170
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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