A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6882659



Internal ID9931190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:89474675..89475016hg38UCSC Ensembl
Outerchr15:90017906..90018247hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750003
Supporting Variants
SamplesSSM094
Known GenesRHCG
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)essv6882659
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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