A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047371



Internal ID21956605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111794788..111794788hg38UCSC Ensembl
chr1:112337410..112337410hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535637
Samples
Known GenesKCND3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047371
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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