A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6094016



Internal ID8943052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70530370..70530494hg38UCSC Ensembl
Outerchr15:70530333..70530544hg38UCSC Ensembl
Innerchr15:70822709..70822833hg19UCSC Ensembl
Outerchr15:70822672..70822883hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2665700
Supporting Variants
SamplesHG00475
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6094016
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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