A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488229



Internal ID21145782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100248261..100409952hg38UCSC Ensembl
chr13:100900515..101062206hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38161692
hg19161692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006737
Samples
Known GenesPCCA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488229
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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