A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110051



Internal ID18930985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:111911905..111911962hg38UCSC Ensembl
Outerchr9:114674185..114674242hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959285
SamplesKWS1
Known GenesUGCG
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110051
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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