A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515256



Internal ID20888615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34425703..34431406hg38UCSC Ensembl
chr17:32752722..32758425hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg385704
hg195704
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515256
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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