A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506311



Internal ID20879589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28246486..28246842hg38UCSC Ensembl
chr17:26573512..26573868hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184057
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506311
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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