A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv206n100



Internal ID20151822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84143663..84207176hg38UCSC Ensembl
chr1:84609346..84672859hg19UCSC Ensembl
chr1:84381934..84445447hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3863514
hg1963514
hg1863514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv997601, nsv1013911, nsv1005225, nsv999772, nsv1002537
Samples
Known GenesPRKACB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv206n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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