A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609465



Internal ID20982536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116654949..116670637hg38UCSC Ensembl
chr7:116295003..116310691hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3815689
hg1915689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149598
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609465
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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