A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660762



Internal ID9926867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119936323..119938016hg38UCSC Ensembl
Innerchr3:119655170..119656863hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg381694
hg191694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv883e199
Supporting Variantsessv6535658, essv5871441, essv6041500, essv6548670, essv5743967
SamplesNA18489, NA19238, NA18516, NA19240, NA19116
Known GenesGSK3B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660762
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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