A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599695



Internal ID6986740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13101246..13106286hg38UCSC Ensembl
Innerchr4:13101246..13106286hg38UCSC Ensembl
Outerchr4:13101018..13106472hg38UCSC Ensembl
chr4:13102870..13107910hg19UCSC Ensembl
Innerchr4:13102870..13107910hg19UCSC Ensembl
Outerchr4:13102642..13108096hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg385041
hg195041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11359148
SamplesHG02137
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599695
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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