A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6944661



Internal ID10053271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:130301195..130301859hg38UCSC Ensembl
Outerchr10:132099459..132100123hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38665
hg19665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2743460, esv2743456
Supporting Variants
SamplesSSM023
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)essv6944661
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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