A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121111



Internal ID19277477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41562715..41564180hg38UCSC Ensembl
Outerchr15:41854913..41856378hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381466
hg191466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3964337
SamplesKWS1
Known GenesTYRO3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121111
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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