A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18175513



Internal ID20742553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18894238..18904578hg38UCSC Ensembl
chr9:18894236..18904576hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3810341
hg1910341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422237
Supporting Variants
Samples
Known GenesADAMTSL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18175513
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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