A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669941



Internal ID9936046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:173994263..173998879hg38UCSC Ensembl
Outerchr1:173994106..173999032hg38UCSC Ensembl
Innerchr1:173963401..173968017hg19UCSC Ensembl
Outerchr1:173963244..173968170hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg384927
hg194927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6240084
SamplesNA19102
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669941
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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