A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6020180



Internal ID9459580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:191608758..191617717hg38UCSC Ensembl
chr3:191326547..191335506hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg388960
hg198960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664831
Supporting Variants
SamplesNA18910
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6020180
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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