A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477539



Internal ID21135092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37100701..37107100hg38UCSC Ensembl
chr13:37674838..37681237hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187512
Samples
Known GenesCSNK1A1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477539
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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