A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18146943



Internal ID20713983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107226338..107238946hg38UCSC Ensembl
chr7:106866783..106879391hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3812609
hg1912609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6605127
Supporting Variants
Samples
Known GenesCOG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18146943
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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