A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657163



Internal ID9923268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:101034736..101039020hg38UCSC Ensembl
chr6:101482612..101486896hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg384285
hg194285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1146e199
Supporting Variantsessv5771929, essv5994187, essv6028485, essv6088284, essv5623495, essv6437653, essv6030849, essv5628507, essv5600109, essv6477448, essv5575961, essv6310321, essv6464589, essv6452800, essv6378183, essv5974087, essv6134472, essv5679929, essv6422541, essv5811522, essv5778693
SamplesNA19700, NA19703, NA18861, NA19819, NA19190, NA19107, NA19379, NA19916, NA19138, NA19471, NA19908, NA19403, NA19236, NA19982, NA18853, NA19473, NA19444, NA19467, NA19248, NA19472, NA19900
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657163
Frequency
Sample Size1151
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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