A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603069



Internal ID6990101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:167519448..167627975hg38UCSC Ensembl
Innerchr4:167519448..167627975hg38UCSC Ensembl
Outerchr4:167518948..167628475hg38UCSC Ensembl
chr4:168440599..168549126hg19UCSC Ensembl
Innerchr4:168440599..168549126hg19UCSC Ensembl
Outerchr4:168440099..168549626hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38108528
hg19108528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11686364
SamplesHG03567
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603069
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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