A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6058572



Internal ID8831438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70095777..70101983hg38UCSC Ensembl
Outerchr15:70095406..70102453hg38UCSC Ensembl
Innerchr15:70388116..70394322hg19UCSC Ensembl
Outerchr15:70387745..70394792hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg387048
hg197048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672644
Supporting Variants
SamplesHG00271
Known GenesTLE3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6058572
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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