A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596453



Internal ID6636724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67274803..67282065hg38UCSC Ensembl
Innerchr3:67274853..67282015hg38UCSC Ensembl
Outerchr3:67274683..67282185hg38UCSC Ensembl
chr3:67325227..67332489hg19UCSC Ensembl
Innerchr3:67325277..67332439hg19UCSC Ensembl
Outerchr3:67325107..67332609hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg387263
hg197263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11030933
SamplesHG01844
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596453
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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