A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509349



Internal ID20882658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32419048..32422111hg38UCSC Ensembl
chr17:30746067..30749130hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg383064
hg193064
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196240
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509349
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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