A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131265



Internal ID18923061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:1291524..1291657hg38UCSC Ensembl
Outerchr5:1291639..1291772hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3021n106
Supporting Variantsnssv3971057
SamplesKWS1
Known GenesTERT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131265
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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