A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14085523



Internal ID21278890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:105874505..105880638hg38UCSC Ensembl
Innerchr7:105514951..105521084hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg386134
hg196134
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113294
Supporting Variants
Samplessample275
Known GenesATXN7L1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14085523
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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