A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557250



Internal ID18508845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14741198..14964965hg38UCSC Ensembl
Innerchr16:14835055..15058822hg19UCSC Ensembl
Innerchr16:14742556..14966323hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38223768
hg19223768
hg18223768
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050163
Supporting Variants
Samples
Known GenesABCC6P2, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO1, NPIPA1, NPIPA2, NPIPA3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3557250
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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