A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv34n100



Internal ID22786121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13980012..14044250hg38UCSC Ensembl
chr1:14306507..14370745hg19UCSC Ensembl
chr1:14179094..14243332hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3864239
hg1964239
hg1864239
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011918, nsv1004214, nsv1001764, nsv1009457, nsv1000636, nsv1006184
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv34n100
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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