A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14252522



Internal ID21305557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2153667..2173309hg38UCSC Ensembl
Outerchr8:2149480..2173516hg38UCSC Ensembl
Innerchr8:2101595..2121238hg19UCSC Ensembl
Outerchr8:2097403..2121444hg19UCSC Ensembl
Innerchr8:2089002..2108645hg18UCSC Ensembl
Outerchr8:2084810..2108851hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3824037
hg1924042
hg1824042
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169893
Supporting Variants
SamplesNGO_21
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14252522
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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