A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3831n54



Internal ID22771726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85960618..86033755hg38UCSC Ensembl
chr14:86426962..86500099hg19UCSC Ensembl
chr14:85496715..85569852hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3873138
hg1973138
hg1873138
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565453, nsv565451, nsv565452
Samples1780854459_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3831n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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