A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6090711



Internal ID9038235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:194025108..194025205hg38UCSC Ensembl
Outerchr3:194025071..194025255hg38UCSC Ensembl
Innerchr3:193742897..193742994hg19UCSC Ensembl
Outerchr3:193742860..193743044hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2666710
Supporting Variants
SamplesHG00672
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6090711
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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