A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058914



Internal ID21968147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77070774..77070774hg38UCSC Ensembl
chr1:77536459..77536459hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531205
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058914
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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