A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247844



Internal ID21311358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68408221..68433309hg38UCSC Ensembl
Outerchr10:68400317..68434797hg38UCSC Ensembl
Innerchr10:70167978..70193066hg19UCSC Ensembl
Outerchr10:70160074..70194554hg19UCSC Ensembl
Innerchr10:69837984..69863072hg18UCSC Ensembl
Outerchr10:69830080..69864560hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3834481
hg1934481
hg1834481
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170113
Supporting Variants
SamplesSNI_1
Known GenesDNA2, RUFY2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247844
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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