A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011579



Internal ID22073210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:18162067..18715910hg38UCSC Ensembl
Outerchr16:18153433..18730788hg38UCSC Ensembl
Innerchr16:18255924..18727232hg19UCSC Ensembl
Outerchr16:18247290..18742110hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38577356
hg19494821
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155258
Supporting Variants
Samples
Known GenesABCC6P1, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO2, NPIPA7, NPIPA8
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011579
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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