A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18160866



Internal ID20727906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81155456..81156125hg38UCSC Ensembl
chr7:80784772..80785441hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612383
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18160866
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00053


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