A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607911



Internal ID20980982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164079501..164146600hg38UCSC Ensembl
chr6:164500533..164567632hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3867100
hg1967100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216994
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607911
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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