A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151078



Internal ID19197262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:74359801..74427702hg38UCSC Ensembl
Outerchr16:74393699..74461600hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3867902
hg1967902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002009
SamplesKWB1
Known GenesCLEC18B, LOC283922
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151078
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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