A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2738374



Internal ID9972714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:72064773..72065247hg38UCSC Ensembl
Outerchr10:73824531..73825005hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6743808, essv6832798, essv6755314, essv6976618
SamplesSSM010, SSM053, SSM029, SSM058
Known GenesSPOCK2
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)esv2738374
Frequency
Sample Size96
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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