A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487043



Internal ID21144596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37461701..37462900hg38UCSC Ensembl
chr13:38035838..38037037hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186434
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487043
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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