A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625324



Internal ID6665471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8936425..8943806hg38UCSC Ensembl
Innerchr11:8936925..8943306hg38UCSC Ensembl
Outerchr11:8935425..8944806hg38UCSC Ensembl
chr11:8957972..8965353hg19UCSC Ensembl
Innerchr11:8958472..8964853hg19UCSC Ensembl
Outerchr11:8956972..8966353hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg387382
hg197382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14020752, essv14020751
SamplesHG02476, NA18622
Known GenesASCL3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625324
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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