A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658390



Internal ID9577809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29791414..29941747hg38UCSC Ensembl
chr6:29759191..29909524hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38150334
hg19150334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1086e199
Supporting Variantsessv6555999, essv6440681, essv6568805, essv6075762
SamplesNA18602, HG00690, NA20522, NA20758
Known GenesHCG4, HCG4B, HLA-G, HLA-H, LOC554223
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658390
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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