A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976796



Internal ID18899799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:70121297..70203697hg38UCSC Ensembl
Outerchr16:70155200..70237600hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3882401
hg1982401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124742
Supporting Variants
SamplesKWS2
Known GenesCLEC18C, PDPR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976796
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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