A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613683



Internal ID7000579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73392101..73398949hg38UCSC Ensembl
Innerchr7:73392601..73398449hg38UCSC Ensembl
Outerchr7:73391101..73399949hg38UCSC Ensembl
chr7:72806431..72813279hg19UCSC Ensembl
Innerchr7:72806931..72812779hg19UCSC Ensembl
Outerchr7:72805431..72814279hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg386849
hg196849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12841019
SamplesHG01849
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613683
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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