A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9741535



Internal ID18715781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:9063687..9063993hg38UCSC Ensembl
Outerchr1:9063631..9064039hg38UCSC Ensembl
Innerchr1:9123746..9124052hg19UCSC Ensembl
Outerchr1:9123690..9124098hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38409
hg19409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3542788
Supporting Variants
Samples
Known GenesSLC2A5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9741535
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