A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2730461



Internal ID9964777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1659805..1660000hg38UCSC Ensembl
Outerchr10:1701999..1702194hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6866670, essv6866669, essv6861924, essv6775370, essv6850590, essv6965171, essv6958632
SamplesSSM027, SSM088, SSM026, SSM089, SSM086, SSM066
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)esv2730461
Frequency
Sample Size96
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer