A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195692



Internal ID20762732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87027128..87027628hg38UCSC Ensembl
chr9:89642043..89642543hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445156
Supporting Variants
Samples
Known GenesLOC440173
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195692
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00066


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