A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6910417



Internal ID10023964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:100445335..100445491hg38UCSC Ensembl
Outerchr2:101061797..101061953hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2720437, esv2720438
Supporting Variants
SamplesSSM015
Known Genes
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)essv6910417
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