A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5708498



Internal ID8893849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10657761..10660647hg38UCSC Ensembl
chr6:10657994..10660880hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg382887
hg192887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666483
Supporting Variants
SamplesHG00343
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5708498
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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