A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595995



Internal ID6983313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42286016..42303539hg38UCSC Ensembl
Innerchr3:42286016..42303539hg38UCSC Ensembl
Outerchr3:42285516..42304039hg38UCSC Ensembl
chr3:42327508..42345031hg19UCSC Ensembl
Innerchr3:42327508..42345031hg19UCSC Ensembl
Outerchr3:42327008..42345531hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3817524
hg1917524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10991716
SamplesNA19726
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595995
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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