A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1953n100



Internal ID20153569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87932015..87949156hg38UCSC Ensembl
chr14:88398359..88415500hg19UCSC Ensembl
chr14:87468112..87485253hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3817142
hg1917142
hg1817142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035754, nsv1046350, nsv1052066, nsv1041023, nsv1051903
Samples
Known GenesGALC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1953n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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