A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598216



Internal ID6985352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152845432..152846992hg38UCSC Ensembl
Innerchr3:152845432..152846992hg38UCSC Ensembl
Outerchr3:152845185..152847301hg38UCSC Ensembl
chr3:152563221..152564781hg19UCSC Ensembl
Innerchr3:152563221..152564781hg19UCSC Ensembl
Outerchr3:152562974..152565090hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg381561
hg191561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11187888, essv11187889, essv11187887
SamplesHG00479, NA18532, NA18636
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598216
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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