A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979337



Internal ID19232885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:1340467..1340564hg38UCSC Ensembl
Outerchr16:1390468..1390565hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1117153
Supporting Variants
SamplesKWS2
Known GenesBAIAP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979337
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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