A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546073



Internal ID18400463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28143589..28143829hg38UCSC Ensembl
Outerchr10:28143569..28143873hg38UCSC Ensembl
Innerchr10:28432518..28432758hg19UCSC Ensembl
Outerchr10:28432498..28432802hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744820
Samples
Known GenesMPP7
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546073
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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