A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662234



Internal ID9928339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:24324588..24328094hg38UCSC Ensembl
Outerchr6:24324217..24328464hg38UCSC Ensembl
Innerchr6:24324816..24328322hg19UCSC Ensembl
Outerchr6:24324445..24328692hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384248
hg194248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1081e199
Supporting Variantsessv5707680, essv5613676, essv5726346, essv5596336, essv5703370, essv6277709, essv6201672, essv5902528, essv6026216, essv5932345, essv5784559, essv5408397, essv6541173, essv5913710, essv6537552, essv5426374, essv5664181, essv5525503, essv5813472, essv5741989, essv6565307, essv5910707, essv5699532
SamplesNA18621, NA18592, NA18526, NA18633, NA18602, NA18627, NA18558, NA18618, NA18571, NA18560, NA18617, NA18605, NA18613, NA18572, NA18534, NA18570, NA18593, NA18608, NA18632, NA18559, NA18628, NA18636, NA18577
Known GenesDCDC2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662234
Frequency
Sample Size1151
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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