A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046810



Internal ID18789341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14957888..15022388hg38UCSC Ensembl
Innerchr16:15051745..15116245hg19UCSC Ensembl
Innerchr16:14959246..15023746hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3864501
hg1964501
hg1864501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2763n100
Supporting Variantsnssv3718975, nssv3718976, nssv3557867, nssv3557868, nssv3557866, nssv3557869, nssv3557865
Samples
Known GenesMIR1972-1, MIR1972-2, PDXDC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046810
Frequency
Sample Size29084
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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