A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156783



Internal ID20723823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19719518..19720073hg38UCSC Ensembl
chr7:19759141..19759696hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6601722
Supporting Variants
Samples
Known GenesTMEM196
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156783
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00029


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