A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602728



Internal ID20975799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109686824..109798706hg38UCSC Ensembl
chr6:110008027..110119909hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38111883
hg19111883
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216798
Samples
Known GenesAK9, FIG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602728
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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