A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677065



Internal ID9943170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3955608..3957580hg38UCSC Ensembl
chr6:3955842..3957814hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381973
hg191973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6370967, essv5972424, essv5987129
SamplesNA19395, NA19390, HG01342
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677065
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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