A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613093



Internal ID20986164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113746063..113758028hg38UCSC Ensembl
chr7:113386118..113398083hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3811966
hg1911966
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230605
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613093
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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