A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14243798



Internal ID21304017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:8122524..8129225hg38UCSC Ensembl
Outerchr1:8116566..8131732hg38UCSC Ensembl
Innerchr1:8182584..8189285hg19UCSC Ensembl
Outerchr1:8176626..8191792hg19UCSC Ensembl
Innerchr1:8105171..8111872hg18UCSC Ensembl
Outerchr1:8099213..8114379hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3815167
hg1915167
hg1815167
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170052
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)nssv14243798
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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