A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616823



Internal ID20989894
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 StatusM
Merged Variants
Supporting Variantsnssv18236768
Samples
Known GenesRBAK, RBAKDN, RBAK-RBAKDN, ZNF890P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616823
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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