A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951113



Internal ID16953300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:22580588..22599587hg38UCSC Ensembl
Outerchr8:22438101..22457100hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3819000
hg1919000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998707
SamplesBILGI_BIOE
Known GenesPDLIM2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951113
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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