A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14240790



Internal ID21306152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68778197..68800838hg38UCSC Ensembl
Outerchr15:68773235..68801835hg38UCSC Ensembl
Innerchr15:69070536..69093177hg19UCSC Ensembl
Outerchr15:69065574..69094174hg19UCSC Ensembl
Innerchr15:66857590..66880231hg18UCSC Ensembl
Outerchr15:66852628..66881228hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3828601
hg1928601
hg1828601
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170072
Supporting Variants
SamplesNGO_25
Known GenesANP32A
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14240790
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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