A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557248



Internal ID18508843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14741198..14960489hg38UCSC Ensembl
Innerchr16:14835055..15054346hg19UCSC Ensembl
Innerchr16:14742556..14961847hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38219292
hg19219292
hg18219292
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043568
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)nssv3557248
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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