A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595242



Internal ID6982560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9559113..9569887hg38UCSC Ensembl
Innerchr3:9559113..9569887hg38UCSC Ensembl
Outerchr3:9558613..9570387hg38UCSC Ensembl
chr3:9600797..9611571hg19UCSC Ensembl
Innerchr3:9600797..9611571hg19UCSC Ensembl
Outerchr3:9600297..9612071hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3810775
hg1910775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10917769
SamplesHG02629
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595242
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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