A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060143



Internal ID18802674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70015881..70105639hg38UCSC Ensembl
Innerchr16:70049784..70139542hg19UCSC Ensembl
Innerchr16:68607285..68697043hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3889759
hg1989759
hg1889759
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3001n100
Supporting Variantsnssv3559494, nssv3722738, nssv3559493, nssv3559491, nssv3559492, nssv3559495, nssv3559497, nssv3559496, nssv3722737, nssv3722739
Samples
Known GenesMIR1972-1, MIR1972-2, PDXDC2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060143
Frequency
Sample Size29084
Observed Gain1
Observed Loss9
Observed Complex0
Frequencyn/a


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