A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671891



Internal ID9937996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91633534..91641016hg38UCSC Ensembl
chr9:94395816..94403298hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg387483
hg197483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5636117, essv5609425, essv5988430, essv5568466, essv6234525, essv6244871, essv6393244, essv5770775, essv6309134, essv6104973, essv6129676
SamplesNA19684, HG01488, HG00173, NA12275, NA20535, HG00268, HG00190, NA06989, NA20828, HG00126, HG00342
Known GenesMIR3910-1, MIR3910-2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671891
Frequency
Sample Size1151
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer