A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675175



Internal ID9941280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12151024..12151435hg38UCSC Ensembl
Outerchr10:12150848..12151588hg38UCSC Ensembl
Innerchr10:12193023..12193434hg19UCSC Ensembl
Outerchr10:12192847..12193587hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6496556, essv6598379, essv5811543, essv5657288, essv6450700, essv6497259, essv5810532, essv6115307
SamplesNA19701, NA19819, NA19381, NA19382, NA18868, NA19247, NA19473, NA19463
Known GenesSEC61A2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675175
Frequency
Sample Size1151
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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