A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628122



Internal ID6668266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132302346..132303739hg38UCSC Ensembl
Innerchr11:132302351..132303734hg38UCSC Ensembl
Outerchr11:132302341..132303744hg38UCSC Ensembl
chr11:132172240..132173633hg19UCSC Ensembl
Innerchr11:132172245..132173628hg19UCSC Ensembl
Outerchr11:132172235..132173638hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381394
hg191394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14317588, essv14317589, essv14317587
SamplesHG00879, HG02390, HG02384
Known GenesNTM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628122
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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