A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18175285



Internal ID20742325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112810941..112812900hg38UCSC Ensembl
chr9:115573221..115575180hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381960
hg191960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437152
Supporting Variants
Samples
Known GenesSNX30
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18175285
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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