A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097967



Internal ID22007200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61667055..61667055hg38UCSC Ensembl
chr10:63426813..63426813hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583519
Samples
Known GenesC10orf107
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097967
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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