A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395615



Internal ID21053168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143358690..143359706hg38UCSC Ensembl
chr5:142738255..142739271hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213233
Samples
Known GenesNR3C1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395615
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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