A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534632



Internal ID20907993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63393492..63438059hg38UCSC Ensembl
chr17:61470853..61515420hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg3844568
hg1944568
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195787
Samples
Known GenesCYB561, TANC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534632
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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