A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959077



Internal ID18866825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:13068743..13069743hg38UCSC Ensembl
Outerchr16:13162600..13163600hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118567
Supporting Variants
SamplesKWS1
Known GenesSHISA9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959077
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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