A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1361n100



Internal ID22787448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8259454..8432064hg38UCSC Ensembl
chr12:8412050..8584660hg19UCSC Ensembl
chr12:8303317..8475927hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38172611
hg19172611
hg18172611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044464, nsv1047103, nsv1037314, nsv1041859, nsv1046598
Samples
Known GenesLINC00937
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1361n100
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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