A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667200



Internal ID9933305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37166933..37221851hg38UCSC Ensembl
chr1:37632534..37687452hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3854919
hg1954919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6547394
SamplesNA19819
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667200
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer