A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6769609



Internal ID10000937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:118197183..118198153hg38UCSC Ensembl
Outerchr10:119956695..119957665hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38971
hg19971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2741484
Supporting Variants
SamplesSSM008
Known GenesCASC2
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)essv6769609
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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