A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132413



Internal ID18902876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:84183448..84198848hg38UCSC Ensembl
Outerchr15:84852200..84867600hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3815401
hg1915401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987188
SamplesKWS1
Known GenesLOC440300
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132413
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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