A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176198



Internal ID20743238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:22752200..22852720hg38UCSC Ensembl
chr9:22752199..22852719hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38100521
hg19100521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431934
Supporting Variants
Samples
Known GenesFLJ35282
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176198
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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