A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037034



Internal ID18779565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14794726..15022388hg38UCSC Ensembl
Innerchr16:14888583..15116245hg19UCSC Ensembl
Innerchr16:14796084..15023746hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38227663
hg19227663
hg18227663
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2746n100
Supporting Variantsnssv3557551, nssv3557547, nssv3557546, nssv3718909, nssv3718910, nssv3557548, nssv3718911, nssv3557550, nssv3557549, nssv3718908
Samples
Known GenesABCC6P2, LOC100288162, MIR1972-1, MIR1972-2, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO1, NPIPA1, PDXDC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037034
Frequency
Sample Size29084
Observed Gain6
Observed Loss4
Observed Complex0
Frequencyn/a


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