A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139651



Internal ID19273327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:29043579..29059279hg38UCSC Ensembl
Outerchr16:29054900..29070600hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3815701
hg1915701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977236
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139651
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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