A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607840



Internal ID20980911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106112701..106115100hg38UCSC Ensembl
chr7:105753147..105755546hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234883
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607840
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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