A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131093



Internal ID18903512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:82526111..82545050hg38UCSC Ensembl
Outerchr15:83194900..83213800hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3818940
hg1918901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3967799
SamplesKWS2
Known GenesCPEB1, RPS17, RPS17L
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131093
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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