A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055498



Internal ID21964731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117837052..117837052hg38UCSC Ensembl
chr1:118379674..118379674hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518927
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055498
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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