A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409273



Internal ID21066826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6295001..6297800hg38UCSC Ensembl
chr6:6295234..6298033hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226034
Samples
Known GenesF13A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409273
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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