A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083647



Internal ID21992880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34979916..34979916hg38UCSC Ensembl
chr15:35272117..35272117hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599136
Samples
Known GenesZNF770
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083647
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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