A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6396719



Internal ID9374122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4099445..4142729hg38UCSC Ensembl
Outerchr3:4099408..4142779hg38UCSC Ensembl
Innerchr3:4141129..4184413hg19UCSC Ensembl
Outerchr3:4141092..4184463hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3843372
hg1943372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676337
Supporting Variants
SamplesNA20542
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6396719
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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