A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12886566



Internal ID2888382
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614106
Supporting Variants
SamplesHG03722
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12886566
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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