A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549811



Internal ID15990534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3044294..3123124hg38UCSC Ensembl
Innerchr10:3086486..3165316hg19UCSC Ensembl
Innerchr10:3076486..3155316hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg3878831
hg1978831
hg1878831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv935n54
Supporting Variantsnssv1174104
SamplesHGDP01085
Known GenesPFKP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549811
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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