A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4834n100



Internal ID20156450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108801003..108939054hg38UCSC Ensembl
chr3:108519850..108657901hg19UCSC Ensembl
chr3:110002540..110140591hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38138052
hg19138052
hg18138052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1014353, nsv999583
Samples
Known GenesGUCA1C, TRAT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4834n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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