A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659136



Internal ID9578555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32553739..32579945hg38UCSC Ensembl
Outerchr6:32553368..32580315hg38UCSC Ensembl
Innerchr6:32521516..32547722hg19UCSC Ensembl
Outerchr6:32521145..32548092hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3826948
hg1926948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1108e199
Supporting Variantsessv5748759, essv5503895, essv5678921, essv6265472, essv6321472, essv5913862, essv5867780, essv5674580, essv5734970, essv5410556, essv6077036, essv6538746, essv5630664, essv5420917, essv6136339, essv5486413, essv6526701, essv5811069, essv5396295, essv6226338, essv5853137, essv6289646, essv5462445, essv6366590, essv5994128, essv5543150, essv6044876, essv6125964, essv6062592, essv6001984, essv6117616, essv5835389, essv6202127, essv5487423, essv5931888
SamplesHG01356, HG01462, HG01359, HG01389, HG01465, HG01461, HG01140, HG01250, HG01350, HG01488, HG01354, HG01365, HG01134, HG01455, HG01495, HG01550, HG01124, HG01353, HG01136, HG01360, HG01498, HG01383, HG01497, HG01148, HG01357, HG01375, HG01494, HG01113, HG01137, HG01342, HG01491, HG01251, HG01377, HG01378, HG01437
Known GenesHLA-DRB1, HLA-DRB6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659136
Frequency
Sample Size1151
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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