A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557235



Internal ID18508830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14617525..14991815hg38UCSC Ensembl
Innerchr16:14711382..15085672hg19UCSC Ensembl
Innerchr16:14618883..14993173hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38374291
hg19374291
hg18374291
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043202
Supporting Variants
Samples
Known GenesABCC6P2, BFAR, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO1, NPIPA1, NPIPA2, NPIPA3, PARN, PDXDC1, PLA2G10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3557235
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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