A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv46n100



Internal ID19010414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16544771..16643493hg38UCSC Ensembl
chr1:16871266..16969988hg19UCSC Ensembl
chr1:16743853..16842575hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3898723
hg1998723
hg1898723
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007618, nsv1001753, nsv1013756
Samples
Known GenesCROCCP2, MIR3675, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv46n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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