A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6894335



Internal ID9941697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1541497..1542889hg38UCSC Ensembl
Outerchr10:1583692..1585084hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg381393
hg191393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2730084
Supporting Variants
SamplesSSM098
Known GenesADARB2, ADARB2-AS1
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)essv6894335
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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