A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111119



Internal ID19268017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:73896202..73896278hg38UCSC Ensembl
Outerchr15:74188543..74188619hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1241n106
Supporting Variantsnssv3962342
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111119
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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