A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6911206



Internal ID9985138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:40125141..40155411hg38UCSC Ensembl
Outerchr15:40417342..40447612hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3830271
hg1930271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2749599
Supporting Variants
SamplesSSM002
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)essv6911206
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