A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951445



Internal ID17300319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:73661566..73685065hg38UCSC Ensembl
Outerchr8:74573801..74597300hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3823500
hg1923500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999298
SamplesBILGI_BIOE
Known GenesSTAU2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951445
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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