A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6260829



Internal ID9238232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25529642..25529783hg38UCSC Ensembl
chr6:25529870..25530011hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2676638
Supporting Variants
SamplesNA18973
Known GenesLRRC16A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6260829
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