A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6788167



Internal ID10192266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:40125091..40155329hg38UCSC Ensembl
Outerchr15:40417292..40447530hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3830239
hg1930239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2749599
Supporting Variants
SamplesSSM069
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)essv6788167
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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