A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2729906



Internal ID9964221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1464447..1464902hg38UCSC Ensembl
Outerchr10:1506642..1507097hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv77e201
Supporting Variantsessv6775365, essv6861920, essv6976430, essv6965164, essv6823271, essv6838277, essv6799838, essv6866663
SamplesSSM083, SSM027, SSM079, SSM088, SSM029, SSM089, SSM066, SSM072
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)esv2729906
Frequency
Sample Size96
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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