A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv166n54



Internal ID20133590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16856620..16955930hg38UCSC Ensembl
chr1:17183115..17282425hg19UCSC Ensembl
chr1:17055702..17155012hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3899311
hg1999311
hg1899311
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv545671, nsv545670
Samples
Known GenesCROCC, MIR3675
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv166n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss5
Observed Complex0
Frequencyn/a


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