A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612013



Internal ID6652228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6074187..6080058hg38UCSC Ensembl
Innerchr7:6074241..6080005hg38UCSC Ensembl
Outerchr7:6074134..6080112hg38UCSC Ensembl
chr7:6113818..6119689hg19UCSC Ensembl
Innerchr7:6113872..6119636hg19UCSC Ensembl
Outerchr7:6113765..6119743hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg385872
hg195872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12672100
SamplesHG00110
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612013
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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