A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1098e199



Internal ID20124400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31388388..31492700hg38UCSC Ensembl
chr6:31356165..31460477hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38104313
hg19104313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2674583, esv2673424
SamplesHG01140, HG00740, NA20276, HG01462, NA19079
Known GenesHCG26, HCP5, MICA
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1098e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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