A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12231587



Internal ID2233403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24811578..24817804hg38UCSC Ensembl
Innerchr6:24812078..24817304hg38UCSC Ensembl
Outerchr6:24810578..24818804hg38UCSC Ensembl
chr6:24811806..24818032hg19UCSC Ensembl
Innerchr6:24812306..24817532hg19UCSC Ensembl
Outerchr6:24810806..24819032hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386227
hg196227
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3608371
Supporting Variants
SamplesNA19327
Known GenesFAM65B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12231587
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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