A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549999



Internal ID15990722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14910793..15018884hg38UCSC Ensembl
Innerchr10:14952792..15060883hg19UCSC Ensembl
Innerchr10:14992798..15100889hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38108092
hg19108092
hg18108092
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv961n54
Supporting Variantsnssv744079
Samples
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549999
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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