A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv744082



Internal ID15691352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14945441..15015375hg38UCSC Ensembl
Innerchr10:14987440..15057374hg19UCSC Ensembl
Innerchr10:15027446..15097380hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3869935
hg1969935
hg1869935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550003
Supporting Variants
Samples
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv744082
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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