A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597052



Internal ID6984366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95686772..95694337hg38UCSC Ensembl
Innerchr3:95687272..95693837hg38UCSC Ensembl
Outerchr3:95685772..95695337hg38UCSC Ensembl
chr3:95405616..95413181hg19UCSC Ensembl
Innerchr3:95406116..95412681hg19UCSC Ensembl
Outerchr3:95404616..95414181hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg387566
hg197566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11070353
SamplesHG03451
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597052
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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