A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221261



Internal ID20788301
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 StatusS
Merged Variantsnsv6435084
Supporting Variants
Samples
Known GenesEQTN, LINC00032, TEK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221261
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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