A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148087



Internal ID19196979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:13571325..13575956hg38UCSC Ensembl
Outerchr9:13571324..13575955hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg384632
hg194632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001594
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148087
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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