A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv149n100



Internal ID20151765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35947159..36032074hg38UCSC Ensembl
chr1:36412760..36497675hg19UCSC Ensembl
chr1:36185347..36270262hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3884916
hg1984916
hg1884916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1008562, nsv1002702
Samples
Known GenesAGO3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv149n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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