A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3754n54



Internal ID22771649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73061922..73082147hg38UCSC Ensembl
chr14:73528630..73548855hg19UCSC Ensembl
chr14:72598383..72618608hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3820226
hg1920226
hg1820226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565091, nsv565082, nsv565074, nsv565084, nsv565077, nsv565086, nsv565068, nsv565081, nsv565067, nsv565087, nsv565057, nsv565066, nsv565080, nsv565083, nsv565065, nsv565095, nsv565056, nsv565073, nsv565069, nsv565094, nsv565090, nsv565092, nsv565076, nsv565085, nsv565072, nsv565078, nsv565079, nsv565060, nsv565093
Samples
Known GenesRBM25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3754n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss76
Observed Complex0
Frequencyn/a


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