A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951547



Internal ID17300421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:38616570..38699669hg38UCSC Ensembl
Outerchr10:38909701..38992800hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3883100
hg1983100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997939
SamplesBILGI_BIOE
Known GenesACTR3BP5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951547
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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