A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145110



Internal ID20712150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71361902..71372619hg38UCSC Ensembl
chr6:72071605..72082322hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3810718
hg1910718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6397970
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145110
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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