A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066120



Internal ID20633160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9537597..9547328hg38UCSC Ensembl
chr1:9597656..9607386hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg389732
hg199731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6328616
Supporting Variants
Samples
Known GenesSLC25A33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066120
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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