A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179129



Internal ID20746169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72014405..72014681hg38UCSC Ensembl
chr9:74629321..74629597hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452249
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179129
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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