A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18160926



Internal ID20727966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81606875..81607308hg38UCSC Ensembl
chr7:81236191..81236624hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609198
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18160926
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00076


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