A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1924n100



Internal ID22788011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:62192490..62242057hg38UCSC Ensembl
chr14:62659208..62708775hg19UCSC Ensembl
chr14:61728961..61778528hg18UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3849568
hg1949568
hg1849568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037586, nsv1044114
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)dgv1924n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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