A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2729573



Internal ID9963888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1205116..1205831hg38UCSC Ensembl
Outerchr10:1251056..1251771hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38716
hg19716
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6873410, essv6720329, essv6862686, essv6927606, essv6716393, essv6775362, essv6845657, essv6904561, essv6830955, essv6779090, essv6895776, essv6809094, essv6838273, essv6935918, essv6749399, essv6740741, essv6783151, essv6968296, essv6787367, essv6806094, essv6684821, essv6771699, essv6923924, essv6958614, essv6948670, essv6799832, essv6768509, essv6795645, essv6897363
SamplesSSM065, SSM013, SSM091, SSM099, SSM043, SSM072, SSM071, SSM024, SSM067, SSM083, SSM005, SSM012, SSM056, SSM085, SSM011, SSM066, SSM003, SSM069, SSM019, SSM052, SSM068, SSM044, SSM074, SSM004, SSM075, SSM026, SSM008, SSM018, SSM081
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)esv2729573
Frequency
Sample Size96
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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