A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966227



Internal ID19216665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41559342..41561123hg38UCSC Ensembl
Outerchr15:41851540..41853321hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381782
hg191782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130307
Supporting Variants
SamplesKWS1
Known GenesTYRO3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966227
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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