A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1887n100



Internal ID22787974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:42430859..42523219hg38UCSC Ensembl
chr14:42900062..42992422hg19UCSC Ensembl
chr14:41969812..42062172hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3892361
hg1992361
hg1892361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051049, nsv1043542
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1887n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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