A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476039



Internal ID21133592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102787325..102788608hg38UCSC Ensembl
chr13:103439675..103440958hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg381284
hg191284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005934
Samples
Known GenesKDELC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476039
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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