A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508143



Internal ID20881441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39152890..39153193hg38UCSC Ensembl
chr17:37309143..37309446hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182482
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508143
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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