A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534663



Internal ID20908024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:48092925..48094115hg38UCSC Ensembl
chr17:46170287..46171477hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg381191
hg191191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036603
Samples
Known GenesCBX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534663
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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