A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397824



Internal ID21055377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5526794..5546483hg38UCSC Ensembl
chr6:5527027..5546716hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3819690
hg1919690
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234416
Samples
Known GenesFARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397824
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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