A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191295



Internal ID20758335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30197700..30502690hg38UCSC Ensembl
chr9:30197698..30502688hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38304991
hg19304991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425727
Supporting Variants
Samples
Known GenesLOC401497
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191295
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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