A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397883



Internal ID21055436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6296701..6300000hg38UCSC Ensembl
chr6:6296934..6300233hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236015
Samples
Known GenesF13A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397883
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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