A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184597



Internal ID20751637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28947892..28948503hg38UCSC Ensembl
chr9:28947890..28948501hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6420035
Supporting Variants
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184597
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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