A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949984



Internal ID17298858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:131740854..131747553hg38UCSC Ensembl
Outerchr8:132753101..132759800hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999325
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949984
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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