A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661445



Internal ID9580864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32962043..32962251hg38UCSC Ensembl
Outerchr3:32962006..32962301hg38UCSC Ensembl
Innerchr3:33003535..33003743hg19UCSC Ensembl
Outerchr3:33003498..33003793hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6441863, essv5437977
SamplesHG01067, HG01082
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661445
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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