A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951566



Internal ID17300440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:43248453..43268652hg38UCSC Ensembl
Outerchr10:43743901..43764100hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3820200
hg1920200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997957
SamplesBILGI_BIOE
Known GenesRASGEF1A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951566
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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