A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154137



Internal ID19195625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:49396002..49402003hg38UCSC Ensembl
Outerchr15:49688199..49694200hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg386002
hg196002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003415
SamplesKWB1
Known GenesFAM227B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1154137
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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