A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18174381



Internal ID20741421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113245327..113249645hg38UCSC Ensembl
chr9:116007607..116011925hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg384319
hg194319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451634
Supporting Variants
Samples
Known GenesSLC31A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18174381
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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