A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951138



Internal ID17300012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:45927979..46010578hg38UCSC Ensembl
Outerchr8:46839601..46922200hg19UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg3882600
hg1982600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999264
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951138
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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