A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049876



Internal ID21959109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23621083..23621083hg38UCSC Ensembl
chr1:23947573..23947573hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38772
hg19772
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529256
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049876
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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