A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5726016



Internal ID8703419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161579327..161661159hg38UCSC Ensembl
chr1:161549117..161630949hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3881833
hg1981833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668992
Supporting Variants
SamplesHG00258
Known GenesFCGR2C, FCGR3B, HSPA7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5726016
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