A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533730



Internal ID20907091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63548001..63560993hg38UCSC Ensembl
chr17:61625362..61638354hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg3812993
hg1912993
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182061
Samples
Known GenesDCAF7, KCNH6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533730
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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