A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479642



Internal ID21137195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100182429..100186769hg38UCSC Ensembl
chr13:100834683..100839023hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg384341
hg194341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006735
Samples
Known GenesPCCA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479642
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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