A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074364



Internal ID21983597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56098440..56098440hg38UCSC Ensembl
chr6:55963238..55963238hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561004
Samples
Known GenesCOL21A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074364
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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