A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664118



Internal ID9930223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32760811..32762810hg38UCSC Ensembl
chr1:33226412..33228411hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6431078
SamplesNA19000
Known GenesKIAA1522
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664118
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