A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661046



Internal ID9927151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:212508432..212509582hg38UCSC Ensembl
Outerchr1:212508395..212509632hg38UCSC Ensembl
Innerchr1:212681774..212682924hg19UCSC Ensembl
Outerchr1:212681737..212682974hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg381238
hg191238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6011124
SamplesHG00656
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661046
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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