A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5994283



Internal ID9389193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:57891851..57893069hg38UCSC Ensembl
Outerchr3:57891814..57893119hg38UCSC Ensembl
Innerchr3:57877578..57878796hg19UCSC Ensembl
Outerchr3:57877541..57878846hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg381306
hg191306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2668341
Supporting Variants
SamplesNA18592
Known GenesSLMAP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5994283
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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