A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153613



Internal ID19199889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:13655414..13655744hg38UCSC Ensembl
Outerchr9:13655413..13655743hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002264
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153613
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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