A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550000



Internal ID15990723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14913179..15018884hg38UCSC Ensembl
Innerchr10:14955178..15060883hg19UCSC Ensembl
Innerchr10:14995184..15100889hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38105706
hg19105706
hg18105706
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv961n54
Supporting Variantsnssv1174127, nssv1174126
Samples1782681109_A, 1780862043_A
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550000
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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