A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6731796



Internal ID9795413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46409113..46410474hg38UCSC Ensembl
Outerchr10:47139277..47140638hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg381362
hg191362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2736240, esv2736152, esv2736163
Supporting Variants
SamplesSSM047
Known GenesLINC00842
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)essv6731796
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