A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596235



Internal ID6636508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57626005..57627619hg38UCSC Ensembl
Innerchr3:57626055..57627569hg38UCSC Ensembl
Outerchr3:57625941..57627683hg38UCSC Ensembl
chr3:57611732..57613346hg19UCSC Ensembl
Innerchr3:57611782..57613296hg19UCSC Ensembl
Outerchr3:57611668..57613410hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg381615
hg191615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11020475
SamplesHG01882
Known GenesDENND6A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596235
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