A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1142868



Internal ID19279033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:94243754..94243826hg38UCSC Ensembl
Outerchr15:94786983..94787055hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3979639, nssv3988101
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1142868
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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