A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5936992



Internal ID9801797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:122240883..122244347hg38UCSC Ensembl
Outerchr3:122240726..122244500hg38UCSC Ensembl
Innerchr3:121959730..121963194hg19UCSC Ensembl
Outerchr3:121959573..121963347hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg383775
hg193775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2677822
Supporting Variants
SamplesNA19835
Known GenesCASR
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5936992
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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