A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951099



Internal ID17299973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:11387992..11393291hg38UCSC Ensembl
Outerchr8:11245501..11250800hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998693
SamplesBILGI_BIOE
Known GenesC8orf12
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951099
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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