A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6936608



Internal ID10042028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:74837268..74837922hg38UCSC Ensembl
Outerchr15:75129609..75130263hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38655
hg19655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2749887
Supporting Variants
SamplesSSM021
Known GenesULK3
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)essv6936608
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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