A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751098



Internal ID18378658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:40529727..40531320hg38UCSC Ensembl
Outerchr15:40529592..40531434hg38UCSC Ensembl
Innerchr15:40821926..40823519hg19UCSC Ensembl
Outerchr15:40821791..40823633hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381843
hg191843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552351
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751098
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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