A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149123



Internal ID19197987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:89916515..89921500hg38UCSC Ensembl
Outerchr9:92678409..92683782hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg384986
hg195374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002632
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149123
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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