A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147255



Internal ID18849869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:1275774..1275894hg38UCSC Ensembl
Outerchr5:1275889..1276009hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000029
SamplesKWB1
Known GenesTERT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147255
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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