A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6327411



Internal ID9304814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:184099582..184101425hg38UCSC Ensembl
Outerchr3:184099425..184101578hg38UCSC Ensembl
Innerchr3:183817370..183819213hg19UCSC Ensembl
Outerchr3:183817213..183819366hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg382154
hg192154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664042
Supporting Variants
SamplesHG00614
Known GenesHTR3E
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6327411
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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