A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490015



Internal ID21147568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19494884..19613279hg38UCSC Ensembl
chr13:20069024..20187419hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38118396
hg19118396
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183400
Samples
Known GenesTPTE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490015
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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