A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173343



Internal ID20740383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:106589801..106594200hg38UCSC Ensembl
chr9:109352082..109356481hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg384400
hg194400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442997
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173343
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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