A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5436770



Internal ID9341556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21761905..21770545hg38UCSC Ensembl
Outerchr3:21761868..21770595hg38UCSC Ensembl
Innerchr3:21803397..21812037hg19UCSC Ensembl
Outerchr3:21803360..21812087hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg388728
hg198728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676494
Supporting Variants
SamplesNA18538
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5436770
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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