A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6857828



Internal ID10255529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:36662489..36662641hg38UCSC Ensembl
Outerchr15:36954690..36954842hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2749571, esv2749572
Supporting Variants
SamplesSSM087
Known GenesC15orf41
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)essv6857828
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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