A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503446



Internal ID20876701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29414072..29422084hg38UCSC Ensembl
chr17:27741090..27749102hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg388013
hg198013
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178192
Samples
Known GenesTAOK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503446
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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