A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6266303



Internal ID9338349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15803663..15805229hg38UCSC Ensembl
chr3:15845170..15846736hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg381567
hg191567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670116
Supporting Variants
SamplesNA18536
Known GenesANKRD28
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6266303
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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