A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524504



Internal ID20897865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70000758..70009249hg38UCSC Ensembl
chr17:67996899..68005390hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg388492
hg198492
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177614
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524504
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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