A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614106



Internal ID6654313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90441809..90478250hg38UCSC Ensembl
Innerchr7:90441809..90478250hg38UCSC Ensembl
Outerchr7:90441309..90478750hg38UCSC Ensembl
chr7:90071123..90107564hg19UCSC Ensembl
Innerchr7:90071123..90107564hg19UCSC Ensembl
Outerchr7:90070623..90108064hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3836442
hg1936442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12886566
SamplesHG03722
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614106
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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