A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6535658



Internal ID9603117
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 Flag1
Merged StatusS
Merged Variantsesv2660762
Supporting Variants
SamplesNA19240
Known GenesGSK3B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6535658
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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