A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18157111



Internal ID20724151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28927841..28940766hg38UCSC Ensembl
chr7:28967458..28980383hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3812926
hg1912926
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616604
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18157111
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00046


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