A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599647



Internal ID6986692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11453237..11505437hg38UCSC Ensembl
Innerchr4:11453237..11505437hg38UCSC Ensembl
Outerchr4:11452737..11505937hg38UCSC Ensembl
chr4:11454861..11507061hg19UCSC Ensembl
Innerchr4:11454861..11507061hg19UCSC Ensembl
Outerchr4:11454361..11507561hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3852201
hg1952201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11357071
SamplesHG01107
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599647
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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