A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511968



Internal ID18810249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14946539..15028134hg38UCSC Ensembl
Innerchr10:14988538..15070133hg19UCSC Ensembl
Innerchr10:15028544..15110139hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3881596
hg1981596
hg1881596
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039755
Supporting Variants
Samples
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3511968
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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