A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6089766



Internal ID9706306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185876571..185880059hg38UCSC Ensembl
chr3:185594359..185597847hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg383489
hg193489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659944
Supporting Variants
SamplesNA19456
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6089766
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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