A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182545



Internal ID20749585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93511184..93512381hg38UCSC Ensembl
chr9:96273466..96274663hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381198
hg191198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444335
Supporting Variants
Samples
Known GenesFAM120A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182545
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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