A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981360



Internal ID19212002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:47143389..47144189hg38UCSC Ensembl
Outerchr16:47177300..47178100hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1144768
Supporting Variants
SamplesKWS1
Known GenesNETO2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981360
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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