A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603520



Internal ID6990551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186081238..186082230hg38UCSC Ensembl
Innerchr4:186081238..186082230hg38UCSC Ensembl
Outerchr4:186080973..186082445hg38UCSC Ensembl
chr4:187002392..187003384hg19UCSC Ensembl
Innerchr4:187002392..187003384hg19UCSC Ensembl
Outerchr4:187002127..187003599hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38993
hg19993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11741732, essv11741733
SamplesNA18615, NA18577
Known GenesTLR3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603520
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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