A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176504



Internal ID20743544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:12278501..12422400hg38UCSC Ensembl
chr9:12278501..12422400hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38143900
hg19143900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432777
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176504
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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