A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7733576



Internal ID13049936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:26586917..26589200hg38UCSC Ensembl
Outerchr11:26586717..26589400hg38UCSC Ensembl
Innerchr11:26608464..26610747hg19UCSC Ensembl
Outerchr11:26608264..26610947hg19UCSC Ensembl
Innerchr11:26565040..26567323hg18UCSC Ensembl
Outerchr11:26564840..26567523hg18UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg382684
hg192684
hg182684
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302858
Supporting Variants
SamplesNA07346
Known GenesANO3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7733576
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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