A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059181



Internal ID21968414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44342857..44342857hg38UCSC Ensembl
chr1:44808529..44808529hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524362
Samples
Known GenesERI3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059181
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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