A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977308



Internal ID19230676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:28599179..28614079hg38UCSC Ensembl
Outerchr16:28610500..28625400hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3814901
hg1914901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115500
Supporting Variants
SamplesKWS2
Known GenesSULT1A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977308
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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