A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051099



Internal ID21960333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201734499..201734499hg38UCSC Ensembl
chr1:201703627..201703627hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533237
Samples
Known GenesIPO9-AS1, NAV1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051099
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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