A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477089



Internal ID21134642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45377001..45383300hg38UCSC Ensembl
chr13:45951136..45957435hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg386300
hg196300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1817n223
Supporting Variantsnssv18185621
Samples
Known GenesTPT1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477089
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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