A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609173



Internal ID20982244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105659325..105661210hg38UCSC Ensembl
chr7:105299772..105301657hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg381886
hg191886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152068
Samples
Known GenesATXN7L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609173
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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