A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5598709



Internal ID9721724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:196592285..196595128hg38UCSC Ensembl
Outerchr3:196592248..196595178hg38UCSC Ensembl
Innerchr3:196319156..196321999hg19UCSC Ensembl
Outerchr3:196319119..196322049hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg382931
hg192931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665949
Supporting Variants
SamplesNA19472
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5598709
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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