A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067414



Internal ID19156633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12405336..12435375hg38UCSC Ensembl
Innerchr19:12516150..12546189hg19UCSC Ensembl
Innerchr19:12377150..12407189hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3830040
hg1930040
hg1830040
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3434n100
Supporting Variantsnssv3564734, nssv3564731, nssv3564727, nssv3564732, nssv3564728, nssv3564733, nssv3564730, nssv3564726, nssv3564729
Samples
Known GenesZNF443
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067414
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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