A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135818



Internal ID19247832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:101214583..101214840hg38UCSC Ensembl
Outerchr15:101754788..101755045hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3989409
SamplesKWS2
Known GenesCHSY1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135818
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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