A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613540



Internal ID20986611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:9317853..9349771hg38UCSC Ensembl
chr7:9357483..9389401hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3831919
hg1931919
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613540
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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