A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv108n100



Internal ID20151724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16850538..17010370hg38UCSC Ensembl
chr1:17177033..17336865hg19UCSC Ensembl
chr1:17049620..17209452hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38159833
hg19159833
hg18159833
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1001977, nsv999404
Samples
Known GenesATP13A2, CROCC, MFAP2, MIR3675
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv108n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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