A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677011



Internal ID9943116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130909798..130917352hg38UCSC Ensembl
Outerchr9:130909761..130917402hg38UCSC Ensembl
Innerchr9:133785185..133792739hg19UCSC Ensembl
Outerchr9:133785148..133792789hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg387642
hg197642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6494207
SamplesNA19003
Known GenesFIBCD1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677011
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