A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14248347



Internal ID21303962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76941965..76944420hg38UCSC Ensembl
Outerchr9:76939544..76951948hg38UCSC Ensembl
Innerchr9:79556881..79559336hg19UCSC Ensembl
Outerchr9:79554460..79566864hg19UCSC Ensembl
Innerchr9:78746701..78749156hg18UCSC Ensembl
Outerchr9:78744280..78756684hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3812405
hg1912405
hg1812405
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169957
Supporting Variants
SamplesNGO_1
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14248347
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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