A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170113



Internal ID21314174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68408221..68446719hg38UCSC Ensembl
Outerchr10:68400317..68450365hg38UCSC Ensembl
Innerchr10:70167978..70206476hg19UCSC Ensembl
Outerchr10:70160074..70210122hg19UCSC Ensembl
Innerchr10:69837984..69876482hg18UCSC Ensembl
Outerchr10:69830080..69880128hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3850049
hg1950049
hg1850049
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247844, nssv14249808
SamplesSNI_8, SNI_1
Known GenesDNA2, RUFY2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170113
Frequency
Sample Size93
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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