A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616634



Internal ID20989705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105765076..105768908hg38UCSC Ensembl
chr7:105405522..105409354hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg383833
hg193833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152076
Samples
Known GenesATXN7L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616634
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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