A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949982



Internal ID17298856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:128915055..128920054hg38UCSC Ensembl
Outerchr8:129927301..129932300hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999323
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949982
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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