A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635595



Internal ID6675708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103476060..103478313hg38UCSC Ensembl
Innerchr14:103476060..103478313hg38UCSC Ensembl
Outerchr14:103475913..103478468hg38UCSC Ensembl
chr14:103942397..103944650hg19UCSC Ensembl
Innerchr14:103942397..103944650hg19UCSC Ensembl
Outerchr14:103942250..103944805hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg382254
hg192254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15114334
SamplesHG01372
Known GenesMARK3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635595
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer