A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061337



Internal ID21970570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123221623..123221623hg38UCSC Ensembl
chr8:124233863..124233863hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582051
Samples
Known GenesC8orf76
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061337
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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