A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6976641



Internal ID10081493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:91528760..91529367hg38UCSC Ensembl
Outerchr10:93288517..93289124hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38608
hg19608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739507
Supporting Variants
SamplesSSM029
Known GenesLOC100188947
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)essv6976641
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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