A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2736263



Internal ID9970595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46218603..46218971hg38UCSC Ensembl
Outerchr10:47589839..47590207hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6705927, essv6799885, essv6948739, essv6728023, essv6691333, essv6838324, essv6702114, essv6677512, essv6906462, essv6884876, essv6970454, essv6701487, essv6779150, essv6894384, essv6720380, essv6819314, essv6890991, essv6915859, essv6976569, essv6672646, essv6834611, essv6896309, essv6787439, essv6695212, essv6760726
SamplesSSM036, SSM083, SSM024, SSM046, SSM097, SSM039, SSM002, SSM028, SSM069, SSM061, SSM029, SSM032, SSM031, SSM067, SSM044, SSM001, SSM040, SSM072, SSM082, SSM078, SSM016, SSM037, SSM095, SSM098, SSM012
Known Genes
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)esv2736263
Frequency
Sample Size96
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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