A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109036



Internal ID18933381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89160373..89160465hg38UCSC Ensembl
Outerchr16:89226781..89226873hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3954870
SamplesKWS1
Known GenesLINC00304
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109036
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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