A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174126



Internal ID15507573
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 StatusS
Merged Variantsnsv550000
Supporting Variants
Samples1780862043_A
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174126
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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