A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6398757



Internal ID9376160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93747286..93748006hg38UCSC Ensembl
chr1:94212842..94213562hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38721
hg19721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657590
Supporting Variants
SamplesNA19468
Known GenesBCAR3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6398757
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