A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751422



Internal ID18725668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73871864..73872042hg38UCSC Ensembl
Outerchr15:73871826..73872083hg38UCSC Ensembl
Innerchr15:74164205..74164383hg19UCSC Ensembl
Outerchr15:74164167..74164424hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552675
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751422
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