A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6677485



Internal ID9744915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:14912757..14913004hg38UCSC Ensembl
Outerchr10:14954756..14955003hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2733495
Supporting Variants
SamplesSSM032
Known GenesDCLRE1C
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)essv6677485
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