A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134444



Internal ID19260348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:47227930..47228037hg38UCSC Ensembl
Outerchr15:47520127..47520234hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3971939
SamplesKWS2
Known GenesSEMA6D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134444
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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