A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036867



Internal ID18779398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:8176904..8428533hg38UCSC Ensembl
Innerchr12:8329500..8581129hg19UCSC Ensembl
Innerchr12:8220767..8472396hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38251630
hg19251630
hg18251630
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1358n100
Supporting Variantsnssv3708224
Samples
Known GenesFAM66C, FAM86FP, FAM90A1, LINC00937, ZNF705A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036867
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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