A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049416



Internal ID21958649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84768823..84768823hg38UCSC Ensembl
chr1:85234506..85234506hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518554
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049416
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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