A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2749294



Internal ID9983578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105437235..105437351hg38UCSC Ensembl
Outerchr14:105903572..105903688hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6857740, essv6966345, essv6828044
SamplesSSM027, SSM087, SSM080
Known GenesMTA1
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)esv2749294
Frequency
Sample Size96
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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