A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6738194



Internal ID10147856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:64340954..64341358hg38UCSC Ensembl
Outerchr15:64633153..64633557hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2749781
Supporting Variants
SamplesSSM050
Known GenesCSNK1G1
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)essv6738194
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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