A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125608



Internal ID18937770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:68397624..68397710hg38UCSC Ensembl
Outerchr15:68689963..68690049hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983787
SamplesKWS2
Known GenesITGA11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125608
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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