A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6677960



Internal ID10091313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:36840330..36840677hg38UCSC Ensembl
Outerchr13:37414467..37414814hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2747269
Supporting Variants
SamplesSSM032
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)essv6677960
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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