A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18147631



Internal ID20714671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9934509..9944667hg38UCSC Ensembl
chr6:9934742..9944900hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3810159
hg1910159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403373
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18147631
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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