A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418380



Internal ID21075933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27067548..27265559hg38UCSC Ensembl
chr9:27067546..27265557hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38198012
hg19198012
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235635
Samples
Known GenesLINC00032, TEK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418380
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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