A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480967



Internal ID21138520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113350847..113586198hg38UCSC Ensembl
chr13:114005162..114240513hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38235352
hg19235352
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177794
Samples
Known GenesADPRHL1, DCUN1D2, GRTP1, TFDP1, TMCO3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480967
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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