A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051525



Internal ID21960758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:68893349..68893349hg38UCSC Ensembl
chr1:69359032..69359032hg19UCSC Ensembl
Cytoband1p31.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523175
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051525
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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