A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201141



Internal ID22350490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105605043..105605486hg38UCSC Ensembl
chr7:105245490..105245933hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14336841
SamplesHG00514
Known GenesATXN7L1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201141
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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