A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037716



Internal ID18780247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:18162067..18737254hg38UCSC Ensembl
Innerchr16:18255924..18748576hg19UCSC Ensembl
Innerchr16:18163425..18656077hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38575188
hg19492653
hg18492653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2782n100
Supporting Variantsnssv3558109
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
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037716
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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