A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18146952



Internal ID20713992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107313635..107328880hg38UCSC Ensembl
chr7:106954080..106969325hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3815246
hg1915246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606801
Supporting Variants
Samples
Known GenesCOG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18146952
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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