A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2729851



Internal ID9964166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1439413..1439875hg38UCSC Ensembl
Outerchr10:1481608..1482070hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6803225, essv6856609, essv6705877, essv6958620, essv6970387, essv6724137, essv6897365, essv6931432, essv6783157, essv6823270, essv6731744, essv6968318, essv6948672, essv6850579
SamplesSSM086, SSM099, SSM040, SSM020, SSM024, SSM045, SSM028, SSM047, SSM073, SSM087, SSM079, SSM068, SSM004, SSM026
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)esv2729851
Frequency
Sample Size96
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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