A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220739



Internal ID20787779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139223801..139231500hg38UCSC Ensembl
chr7:138908547..138916246hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg387700
hg197700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422158
Supporting Variants
Samples
Known GenesUBN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220739
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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