A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231832



Internal ID20798872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113232787..113233156hg38UCSC Ensembl
chr9:115995067..115995436hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451450
Supporting Variants
Samples
Known GenesSLC31A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231832
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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