A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663905



Internal ID9583324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40695514..40696117hg38UCSC Ensembl
chr1:41161186..41161789hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5524790
SamplesNA19679
Known GenesNFYC
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663905
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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