A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3898n54



Internal ID22771793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100527708..100617621hg38UCSC Ensembl
chr14:100994045..101083958hg19UCSC Ensembl
chr14:100063798..100153711hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3889914
hg1989914
hg1889914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565782, nsv565783
SamplesNINDS_61
Known GenesBEGAIN, WDR25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3898n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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