A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9750960



Internal ID18725206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24872019..24873353hg38UCSC Ensembl
Outerchr15:24871696..24873690hg38UCSC Ensembl
Innerchr15:25117166..25118500hg19UCSC Ensembl
Outerchr15:25116843..25118837hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381995
hg191995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552213
Supporting Variants
Samples
Known GenesSNRPN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9750960
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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