A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098704



Internal ID21288121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77957052..77962089hg38UCSC Ensembl
Innerchr17:75953134..75958171hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg385038
hg195038
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115231
Supporting Variants
Samplessample412
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098704
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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