A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564888



Internal ID7035988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:100214125..100220776hg38UCSC Ensembl
Outerchr14:100680462..100687113hg19UCSC Ensembl
Outerchr14:99750215..99756866hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg386652
hg196652
hg186652
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv990695
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564888
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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