A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037379



Internal ID18779910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14959856..15022388hg38UCSC Ensembl
Innerchr16:15053713..15116245hg19UCSC Ensembl
Innerchr16:14961214..15023746hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3862533
hg1962533
hg1862533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2763n100
Supporting Variantsnssv3557884, nssv3557883, nssv3557885, nssv3557882
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)nsv1037379
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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