A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5805914



Internal ID8783317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:174440926..174441032hg38UCSC Ensembl
Outerchr3:174440555..174441402hg38UCSC Ensembl
Innerchr3:174158716..174158822hg19UCSC Ensembl
Outerchr3:174158345..174159192hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38848
hg19848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659795
Supporting Variants
SamplesNA10847
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5805914
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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