A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11238193



Internal ID6338846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177922862..177929476hg38UCSC Ensembl
Innerchr3:177923184..177929154hg38UCSC Ensembl
Outerchr3:177922540..177929798hg38UCSC Ensembl
chr3:177640650..177647264hg19UCSC Ensembl
Innerchr3:177640972..177646942hg19UCSC Ensembl
Outerchr3:177640328..177647586hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg386615
hg196615
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598807
Supporting Variants
SamplesNA20126
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11238193
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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