A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18161211



Internal ID20728251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87306301..87319800hg38UCSC Ensembl
chr7:86935617..86949116hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3813500
hg1913500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603422
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18161211
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01886


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