A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2722895



Internal ID10306531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:217323448..217324277hg38UCSC Ensembl
Outerchr1:217496790..217497619hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38830
hg19830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6777090, essv6750054, essv6972646, essv6699776, essv6669222, essv6722157
SamplesSSM008, SSM045, SSM039, SSM029, SSM031, SSM067
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)esv2722895
Frequency
Sample Size96
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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