A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656904



Internal ID9576323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:97762580..97776701hg38UCSC Ensembl
Outerchr3:97762423..97776854hg38UCSC Ensembl
Innerchr3:97481424..97495545hg19UCSC Ensembl
Outerchr3:97481267..97495698hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3814432
hg1914432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5644484
SamplesHG00613
Known GenesARL6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656904
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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