A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18148168



Internal ID20715208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76261705..76264356hg38UCSC Ensembl
chr6:76971422..76974073hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg382652
hg192652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396482
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18148168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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