A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659885



Internal ID9579304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99956551..99962758hg38UCSC Ensembl
chr6:100404427..100410634hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg386208
hg196208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5929011
SamplesNA19921
Known GenesMCHR2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659885
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