A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049509



Internal ID21958742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85227969..85227969hg38UCSC Ensembl
chr1:85693652..85693652hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522372
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049509
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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