A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109966



Internal ID19269019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:35271276..35271336hg38UCSC Ensembl
Outerchr8:35128794..35128854hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3958418
SamplesKWS1
Known GenesUNC5D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109966
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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