A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403988



Internal ID21061541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55363401..55369900hg38UCSC Ensembl
chr6:55228199..55234698hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6189n223
Supporting Variantsnssv18235939
Samples
Known GenesGFRAL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403988
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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