A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18161208



Internal ID20728248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87287883..87337489hg38UCSC Ensembl
chr7:86917199..86966805hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3849607
hg1949607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612386
Supporting Variants
Samples
Known GenesTP53TG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18161208
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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