A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507618



Internal ID20880912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19503357..19507194hg38UCSC Ensembl
chr17:19406670..19410507hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg383838
hg193838
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193580
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507618
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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