A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174133



Internal ID15854887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14948370..15018884hg38UCSC Ensembl
Innerchr10:14990369..15060883hg19UCSC Ensembl
Innerchr10:15030375..15100889hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3870515
hg1970515
hg1870515
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550007
Supporting Variants
Samples1780862378_A
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174133
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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