A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6527419



Internal ID9265997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:49448841..49532906hg38UCSC Ensembl
chr1:49914513..49998578hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3884066
hg1984066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662284
Supporting Variants
SamplesNA12341
Known GenesAGBL4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6527419
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