A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6093333



Internal ID9586187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62663408..62664798hg38UCSC Ensembl
Outerchr15:62663251..62664951hg38UCSC Ensembl
Innerchr15:62955607..62956997hg19UCSC Ensembl
Outerchr15:62955450..62957150hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381701
hg191701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2672262
Supporting Variants
SamplesNA19190
Known GenesTLN2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6093333
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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