A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3429235



Internal ID15276191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73232419..73232461hg38UCSC Ensembl
Innerchr11:73232426..73232454hg38UCSC Ensembl
Outerchr11:73232412..73232468hg38UCSC Ensembl
chr11:72943464..72943506hg19UCSC Ensembl
Innerchr11:72943471..72943499hg19UCSC Ensembl
Outerchr11:72943457..72943513hg19UCSC Ensembl
chr11:72621112..72621154hg18UCSC Ensembl
Innerchr11:72621119..72621147hg18UCSC Ensembl
Outerchr11:72621105..72621161hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3857
hg1957
hg1857
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7865493
SamplesNA12005
Known GenesP2RY2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3429235
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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