A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598807



Internal ID6985942
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11238190, essv11238193, essv11238192, essv11238191, essv11238189
SamplesNA19209, HG03583, NA20126, HG02501, HG03439
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598807
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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