A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550390



Internal ID16337799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34210719..34274997hg38UCSC Ensembl
Innerchr10:34499647..34563925hg19UCSC Ensembl
Innerchr10:34539653..34603931hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3864279
hg1964279
hg1864279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174973
Samples1788485381_A
Known GenesPARD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550390
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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