A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236768



Internal ID20803808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5021692..5168032hg38UCSC Ensembl
chr7:5061323..5207663hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38146341
hg19146341
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616823
Supporting Variants
Samples
Known GenesRBAK, RBAKDN, RBAK-RBAKDN, ZNF890P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236768
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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