A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487933



Internal ID21145486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67049718..67050477hg38UCSC Ensembl
chr13:67623850..67624609hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38760
hg19760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012099
Samples
Known GenesPCDH9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487933
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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