A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6696006



Internal ID10108261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:68757252..68757551hg38UCSC Ensembl
Outerchr15:69049591..69049890hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2749820
Supporting Variants
SamplesSSM037
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)essv6696006
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