A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518062



Internal ID20891423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61000886..61059841hg38UCSC Ensembl
chr17:59078247..59137202hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3858956
hg1958956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036803
Samples
Known GenesBCAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518062
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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