A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6959757



Internal ID9715437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:63752163..63752498hg38UCSC Ensembl
Outerchr14:64218881..64219216hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2748780, esv2748779
Supporting Variants
SamplesSSM026
Known Genes
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6959757
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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