A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670825



Internal ID9936930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151421569..151422285hg38UCSC Ensembl
chr4:152342721..152343437hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6512964, essv6065877, essv6193591, essv6112795, essv6328917, essv5432670, essv6336128
SamplesHG00262, HG00264, HG00260, NA12829, HG01107, NA06986, HG00252
Known GenesFAM160A1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670825
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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