A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011104



Internal ID22072735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68156309..68175145hg38UCSC Ensembl
Outerchr15:68145377..68179512hg38UCSC Ensembl
Innerchr15:68448647..68467483hg19UCSC Ensembl
Outerchr15:68437715..68471850hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3834136
hg1934136
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155187
Supporting Variants
Samples
Known GenesPIAS1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011104
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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