A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv101n100



Internal ID20151717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16756084..16959812hg38UCSC Ensembl
chr1:17082579..17286307hg19UCSC Ensembl
chr1:16955166..17158894hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38203729
hg19203729
hg18203729
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1013757, nsv1010868, nsv997704, nsv997588, nsv1012064, nsv1006989, nsv997522, nsv1010245, nsv1005424, nsv1014863, nsv1008997, nsv1004987, nsv999848, nsv1001823
Samples
Known GenesCROCC, MIR3675, MST1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv101n100
Frequency
Sample Size29084
Observed Gain23
Observed Loss0
Observed Complex0
Frequencyn/a


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