A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663339



Internal ID9582758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:106876545..106900932hg38UCSC Ensembl
Outerchr3:106876508..106900982hg38UCSC Ensembl
Innerchr3:106595392..106619779hg19UCSC Ensembl
Outerchr3:106595355..106619829hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3824475
hg1924475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6196762, essv6592817
SamplesNA19901, NA19908
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663339
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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