A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097947



Internal ID21280503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:76352277..76355144hg38UCSC Ensembl
Innerchr17:74348358..74351225hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg382868
hg192868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111871
Supporting Variants
Samplessample3
Known GenesPRPSAP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097947
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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