A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11636832



Internal ID3039236
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602475
Supporting Variants
SamplesHG02676
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11636832
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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