A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6354004



Internal ID8798693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:107638159..107640660hg38UCSC Ensembl
Outerchr3:107638122..107640718hg38UCSC Ensembl
Innerchr3:107357006..107359507hg19UCSC Ensembl
Outerchr3:107356969..107359565hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg382597
hg192597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2670666
Supporting Variants
SamplesHG00245
Known GenesBBX
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6354004
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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