A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18010827



Internal ID20577867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61411357..61412082hg38UCSC Ensembl
chr13:61985490..61986215hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38726
hg19726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483417
Supporting Variants
Samples
Known GenesPCDH20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18010827
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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