A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428519



Internal ID21086072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157393266..157427702hg38UCSC Ensembl
chr7:157185960..157220396hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3834437
hg1934437
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224501
Samples
Known GenesDNAJB6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428519
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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