A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094979



Internal ID22004212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68697437..68697437hg38UCSC Ensembl
chr17:66693578..66693578hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627258
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094979
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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