A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596289



Internal ID6983606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59888393..60159064hg38UCSC Ensembl
Innerchr3:59888409..60159048hg38UCSC Ensembl
Outerchr3:59888377..60159080hg38UCSC Ensembl
chr3:59874119..60144792hg19UCSC Ensembl
Innerchr3:59874135..60144776hg19UCSC Ensembl
Outerchr3:59874103..60144808hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38270672
hg19270674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11025670
SamplesHG03667
Known GenesFHIT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596289
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