A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5866369



Internal ID9660683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15761710..15774686hg38UCSC Ensembl
chr6:15761941..15774917hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3812977
hg1912977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661920
Supporting Variants
SamplesNA19393
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5866369
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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