A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6113958



Internal ID9263207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:19814703..19820962hg38UCSC Ensembl
Outerchr6:19814546..19821115hg38UCSC Ensembl
Innerchr6:19814934..19821193hg19UCSC Ensembl
Outerchr6:19814777..19821346hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386570
hg196570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670227
Supporting Variants
SamplesNA12286
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6113958
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