A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138359



Internal ID18937198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41570340..41570603hg38UCSC Ensembl
Outerchr15:41862538..41862801hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990920
SamplesKWS2
Known GenesTYRO3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138359
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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