A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625435



Internal ID7012269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15445833..15448010hg38UCSC Ensembl
Innerchr11:15445842..15448002hg38UCSC Ensembl
Outerchr11:15445825..15448019hg38UCSC Ensembl
chr11:15467379..15469556hg19UCSC Ensembl
Innerchr11:15467388..15469548hg19UCSC Ensembl
Outerchr11:15467371..15469565hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg382178
hg192178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14034626
SamplesNA19017
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625435
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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