A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397141



Internal ID21054694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6298001..6299800hg38UCSC Ensembl
chr6:6298234..6300033hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232246
Samples
Known GenesF13A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397141
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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