A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435084



Internal ID21092637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27220362..27288681hg38UCSC Ensembl
chr9:27220360..27288679hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3868320
hg1968320
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221261
Samples
Known GenesEQTN, LINC00032, TEK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435084
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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