A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5985782



Internal ID9108966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60292427..60292744hg38UCSC Ensembl
chr8:61204986..61205303hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2664491
Supporting Variants
SamplesHG01102
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5985782
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer