A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12826564



Internal ID3468559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:68086388..68090441hg38UCSC Ensembl
chr7:67551375..67555428hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg384054
hg194054
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3613567
Supporting Variants
SamplesHG03086
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12826564
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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