A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6064085



Internal ID9703664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100503663..100504374hg38UCSC Ensembl
chr15:101043868..101044579hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38712
hg19712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674387
Supporting Variants
SamplesNA19453
Known GenesCERS3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6064085
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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