A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598952



Internal ID6986000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184585617..184587518hg38UCSC Ensembl
Innerchr3:184585617..184587518hg38UCSC Ensembl
Outerchr3:184585477..184587716hg38UCSC Ensembl
chr3:184303405..184305306hg19UCSC Ensembl
Innerchr3:184303405..184305306hg19UCSC Ensembl
Outerchr3:184303265..184305504hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg381902
hg191902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11257565, essv11257564, essv11257567, essv11257569, essv11257568, essv11257566
SamplesHG00736, HG00281, NA19670, NA07051, HG00123, NA20528
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598952
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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