A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987193



Internal ID18857899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:14985343..15030443hg38UCSC Ensembl
Outerchr16:15079200..15124300hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3845101
hg1945101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132417
Supporting Variants
SamplesKWS1
Known GenesPDXDC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987193
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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