A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663023



Internal ID9929128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:215481069..215482689hg38UCSC Ensembl
Outerchr1:215480912..215482842hg38UCSC Ensembl
Innerchr1:215654412..215656032hg19UCSC Ensembl
Outerchr1:215654255..215656185hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg381931
hg191931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6290186
SamplesHG00334
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663023
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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