A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18174681



Internal ID20741721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130267101..130272500hg38UCSC Ensembl
chr9:133029380..133034779hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455450
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18174681
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.08136


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