A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665848



Internal ID9931953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119936323..119938013hg38UCSC Ensembl
chr3:119655170..119656860hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg381691
hg191691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv883e199
Supporting Variantsessv5978288, essv6501121
SamplesNA19908, NA19462
Known GenesGSK3B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665848
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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