A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105642



Internal ID22014875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37677771..37677771hg38UCSC Ensembl
chr21:39050073..39050073hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640752
Samples
Known GenesKCNJ6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105642
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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