A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614665



Internal ID7001558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114732773..114739617hg38UCSC Ensembl
Innerchr7:114732820..114739571hg38UCSC Ensembl
Outerchr7:114732727..114739664hg38UCSC Ensembl
chr7:114372828..114379672hg19UCSC Ensembl
Innerchr7:114372875..114379626hg19UCSC Ensembl
Outerchr7:114372782..114379719hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg386845
hg196845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12932537, essv12932538
SamplesHG00306, NA20812
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614665
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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