A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671008



Internal ID9590427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:156396526..156399113hg38UCSC Ensembl
Outerchr1:156396369..156399266hg38UCSC Ensembl
Innerchr1:156366318..156368905hg19UCSC Ensembl
Outerchr1:156366161..156369058hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg382898
hg192898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6283663
SamplesNA18573
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671008
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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