A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035321



Internal ID18777852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:18148857..18751122hg38UCSC Ensembl
Innerchr16:18242714..18762444hg19UCSC Ensembl
Innerchr16:18150215..18669945hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38602266
hg19519731
hg18519731
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2783n100
Supporting Variantsnssv3558104, nssv3558103, nssv3716920
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)nsv1035321
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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