A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3626n54



Internal ID22771521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35137604..35141070hg38UCSC Ensembl
chr14:35606810..35610276hg19UCSC Ensembl
chr14:34676561..34680027hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg383467
hg193467
hg183467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564298, nsv564303, nsv564296, nsv564300, nsv564297
Samples
Known GenesKIAA0391
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3626n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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