A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751170



Internal ID18378730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:49252700..49255382hg38UCSC Ensembl
Outerchr15:49252607..49255864hg38UCSC Ensembl
Innerchr15:49544897..49547579hg19UCSC Ensembl
Outerchr15:49544804..49548061hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg383258
hg193258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552423
Supporting Variants
Samples
Known GenesGALK2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751170
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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