A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602475



Internal ID6989509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141979163..141985331hg38UCSC Ensembl
Innerchr4:141979663..141984831hg38UCSC Ensembl
Outerchr4:141978163..141986331hg38UCSC Ensembl
chr4:142900316..142906484hg19UCSC Ensembl
Innerchr4:142900816..142905984hg19UCSC Ensembl
Outerchr4:142899316..142907484hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg386169
hg196169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11636833, essv11636832
SamplesHG03108, HG02676
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602475
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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