A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622742



Internal ID6662911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28275692..28283742hg38UCSC Ensembl
Innerchr10:28275692..28283742hg38UCSC Ensembl
Outerchr10:28275332..28284121hg38UCSC Ensembl
chr10:28564621..28572671hg19UCSC Ensembl
Innerchr10:28564621..28572671hg19UCSC Ensembl
Outerchr10:28564261..28573050hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg388051
hg198051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13737836, essv13737840, essv13737841, essv13737829, essv13737833, essv13737844, essv13737827, essv13737828, essv13737838, essv13737830, essv13737826, essv13737848, essv13737834, essv13737847, essv13737831, essv13737835, essv13737837, essv13737846, essv13737843, essv13737839, essv13737825, essv13737832, essv13737845, essv13737842
SamplesHG02330, HG03280, NA19437, HG01205, NA19093, HG03055, NA19149, NA18489, HG01182, NA19108, HG03162, HG03484, HG02012, NA18856, NA19908, HG01879, NA19457, NA19332, HG02339, HG03132, NA19446, HG03123, HG03271, HG00641
Known GenesMPP7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622742
Frequency
Sample Size2504
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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