A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002516



Internal ID21911859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:79827240..79901555hg38UCSC Ensembl
chr6:80536957..80611272hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3874316
hg1974316
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572093
Samples
Known GenesC6orf7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002516
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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