A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14249808



Internal ID21313285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68414675..68446719hg38UCSC Ensembl
Outerchr10:68410900..68450365hg38UCSC Ensembl
Innerchr10:70174432..70206476hg19UCSC Ensembl
Outerchr10:70170657..70210122hg19UCSC Ensembl
Innerchr10:69844438..69876482hg18UCSC Ensembl
Outerchr10:69840663..69880128hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3839466
hg1939466
hg1839466
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170113
Supporting Variants
SamplesSNI_8
Known GenesDNA2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14249808
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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