A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600265



Internal ID6640529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38799995..38801448hg38UCSC Ensembl
Innerchr4:38799995..38801448hg38UCSC Ensembl
Outerchr4:38799707..38801748hg38UCSC Ensembl
chr4:38801616..38803069hg19UCSC Ensembl
Innerchr4:38801616..38803069hg19UCSC Ensembl
Outerchr4:38801328..38803369hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381454
hg191454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11397814, essv11397813
SamplesHG02017, HG01857
Known GenesTLR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600265
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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