A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18144992



Internal ID20712032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:50807067..50810186hg38UCSC Ensembl
chr6:50774780..50777899hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg383120
hg193120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413293
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18144992
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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