A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598799



Internal ID6985934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177485436..177494423hg38UCSC Ensembl
Innerchr3:177485450..177494410hg38UCSC Ensembl
Outerchr3:177485423..177494437hg38UCSC Ensembl
chr3:177203224..177212211hg19UCSC Ensembl
Innerchr3:177203238..177212198hg19UCSC Ensembl
Outerchr3:177203211..177212225hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg388988
hg198988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11237613
SamplesHG02855
Known GenesLINC00578
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598799
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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