A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989409



Internal ID19239042
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 StatusS
Merged Variantsnsv1135818
Supporting Variants
SamplesKWS2
Known GenesCHSY1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989409
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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