A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227751



Internal ID20794791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6294801..6303700hg38UCSC Ensembl
chr6:6295034..6303933hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg388900
hg198900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401782
Supporting Variants
Samples
Known GenesF13A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227751
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00014


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