A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6227892



Internal ID8981403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78285407..78287706hg38UCSC Ensembl
chr17:76281488..76283787hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669581
Supporting Variants
SamplesHG00566
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6227892
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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