A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6677558



Internal ID10091697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97829681..97830017hg38UCSC Ensembl
Outerchr10:99589438..99589774hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739940
Supporting Variants
SamplesSSM032
Known GenesLINC00866
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)essv6677558
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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