A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12895714



Internal ID3270710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93803166..93838113hg38UCSC Ensembl
chr7:93432478..93467425hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3834948
hg1934948
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614173
Supporting Variants
SamplesHG02887
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12895714
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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