A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6850578



Internal ID9902316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1438810..1439022hg38UCSC Ensembl
Outerchr10:1481005..1481217hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2729840, esv2729829
Supporting Variants
SamplesSSM086
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)essv6850578
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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