A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179230



Internal ID20746270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30244465..30487669hg38UCSC Ensembl
chr9:30244463..30487667hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38243205
hg19243205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426280
Supporting Variants
Samples
Known GenesLOC401497
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179230
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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