A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2738363



Internal ID10321999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:71949357..71963224hg38UCSC Ensembl
Outerchr10:73709115..73722982hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3813868
hg1913868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6685365, essv6832787
SamplesSSM005, SSM010
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)esv2738363
Frequency
Sample Size96
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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