A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744554



Internal ID18718800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4827322..4827499hg38UCSC Ensembl
Outerchr10:4827298..4827516hg38UCSC Ensembl
Innerchr10:4869514..4869691hg19UCSC Ensembl
Outerchr10:4869490..4869708hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545807
Supporting Variants
Samples
Known GenesAKR1E2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744554
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