A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603216



Internal ID6990248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173712010..173714384hg38UCSC Ensembl
Innerchr4:173712022..173714373hg38UCSC Ensembl
Outerchr4:173711999..173714396hg38UCSC Ensembl
chr4:174633161..174635535hg19UCSC Ensembl
Innerchr4:174633173..174635524hg19UCSC Ensembl
Outerchr4:174633150..174635547hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg382375
hg192375
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11708524
SamplesHG02408
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603216
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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