A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18130781



Internal ID20697821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39323019..39324789hg38UCSC Ensembl
chr5:39323121..39324891hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg381771
hg191771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6378204
Supporting Variants
Samples
Known GenesC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18130781
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00028


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