A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035319



Internal ID18777850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:25867734..25944215hg38UCSC Ensembl
Innerchr12:26020667..26097148hg19UCSC Ensembl
Innerchr12:25911934..25988415hg18UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3876482
hg1976482
hg1876482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710334
Samples
Known GenesMIR4302
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035319
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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