A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6665348



Internal ID10077278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:74991027..74991133hg38UCSC Ensembl
Outerchr15:75283368..75283474hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2749891, esv2749892
Supporting Variants
SamplesSSM029
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)essv6665348
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