A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061307



Internal ID21970540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2578169..2578169hg38UCSC Ensembl
chr6:2578403..2578403hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571449
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061307
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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