A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140514



Internal ID20707555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167139440..167141450hg38UCSC Ensembl
chr6:167552928..167554938hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382011
hg192011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610751
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140514
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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