A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6779091



Internal ID9837977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1373727..1374057hg38UCSC Ensembl
Outerchr10:1415922..1416252hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2729740
Supporting Variants
SamplesSSM067
Known GenesADARB2
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)essv6779091
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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