A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14014306



Internal ID4430659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7368890..7374357hg38UCSC Ensembl
Innerchr11:7368890..7374357hg38UCSC Ensembl
Outerchr11:7368714..7374528hg38UCSC Ensembl
chr11:7390121..7395588hg19UCSC Ensembl
Innerchr11:7390121..7395588hg19UCSC Ensembl
Outerchr11:7389945..7395759hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385468
hg195468
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625289
Supporting Variants
SamplesHG03943
Known GenesSYT9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14014306
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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