A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092620



Internal ID22001853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76841385..76841385hg38UCSC Ensembl
chr17:74837467..74837467hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626660
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092620
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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