A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6752666



Internal ID10160584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:39360089..39361344hg38UCSC Ensembl
Outerchr13:39934226..39935481hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381256
hg191256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2747287
Supporting Variants
SamplesSSM057
Known GenesLHFP
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)essv6752666
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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