A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744683



Internal ID18372243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14199816..14200427hg38UCSC Ensembl
Outerchr10:14199693..14200501hg38UCSC Ensembl
Innerchr10:14241815..14242426hg19UCSC Ensembl
Outerchr10:14241692..14242500hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38809
hg19809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545936
Supporting Variants
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744683
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