A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5574026



Internal ID9902008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:140151640..140154409hg38UCSC Ensembl
Outerchr3:140151603..140154459hg38UCSC Ensembl
Innerchr3:139870482..139873251hg19UCSC Ensembl
Outerchr3:139870445..139873301hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg382857
hg192857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676006
Supporting Variants
SamplesNA20796
Known GenesCLSTN2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5574026
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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