A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550019



Internal ID15990742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:16463718..16478785hg38UCSC Ensembl
Innerchr10:16505717..16520784hg19UCSC Ensembl
Innerchr10:16545723..16560790hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3815068
hg1915068
hg1815068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174136
SamplesHGDP00747
Known GenesPTER
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550019
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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