A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14244918



Internal ID21307147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10649361..10680025hg38UCSC Ensembl
Outerchr9:10645614..10681443hg38UCSC Ensembl
Innerchr9:10649361..10680025hg19UCSC Ensembl
Outerchr9:10645614..10681443hg19UCSC Ensembl
Innerchr9:10639361..10670025hg18UCSC Ensembl
Outerchr9:10635614..10671443hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3835830
hg1935830
hg1835830
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169680
Supporting Variants
SamplesNGO_32
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14244918
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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