A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3631n54



Internal ID22771526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35533726..35535507hg38UCSC Ensembl
chr14:36002932..36004713hg19UCSC Ensembl
chr14:35072683..35074464hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg381782
hg191782
hg181782
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564324, nsv564329, nsv564328
Samples
Known GenesINSM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3631n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss4
Observed Complex0
Frequencyn/a


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