A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535089



Internal ID20908450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10198679..10199867hg38UCSC Ensembl
chr20:10179327..10180515hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg381189
hg191189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066221
Samples
Known GenesSNAP25-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535089
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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