A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171579



Internal ID20738619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100807651..100810182hg38UCSC Ensembl
chr9:103569933..103572464hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg382532
hg192532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451923
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171579
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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