A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595921



Internal ID6983239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39157242..39174647hg38UCSC Ensembl
Innerchr3:39157242..39174647hg38UCSC Ensembl
Outerchr3:39156742..39175147hg38UCSC Ensembl
chr3:39198733..39216138hg19UCSC Ensembl
Innerchr3:39198733..39216138hg19UCSC Ensembl
Outerchr3:39198233..39216638hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3817406
hg1917406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10987598, essv10987597
SamplesNA18947, NA18959
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595921
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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