A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115090



Internal ID18926784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:39696268..39696320hg38UCSC Ensembl
Outerchr8:39553787..39553839hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975392
SamplesKWS2
Known GenesADAM18
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115090
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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