A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3775n54



Internal ID22771670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73769024..73778904hg38UCSC Ensembl
chr14:74235727..74245607hg19UCSC Ensembl
chr14:73305480..73315360hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg389881
hg199881
hg189881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565174, nsv565173
Samples
Known GenesELMSAN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3775n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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