A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633808



Internal ID7020614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24502329..24527587hg38UCSC Ensembl
Innerchr14:24502329..24527587hg38UCSC Ensembl
Outerchr14:24501829..24528087hg38UCSC Ensembl
chr14:24971535..24996793hg19UCSC Ensembl
Innerchr14:24971535..24996793hg19UCSC Ensembl
Outerchr14:24971035..24997293hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3825259
hg1925259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14942628
SamplesNA18561
Known GenesCMA1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633808
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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