A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18172662



Internal ID20739702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104403515..104403923hg38UCSC Ensembl
chr9:107165796..107166204hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38409
hg19409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442724
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18172662
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00152


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