A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059540



Internal ID21968773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19877081..19877081hg38UCSC Ensembl
chr2:20076842..20076842hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517867
Samples
Known GenesLINC00954
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059540
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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