A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595571



Internal ID6635845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24121599..24129827hg38UCSC Ensembl
Innerchr3:24121599..24129827hg38UCSC Ensembl
Outerchr3:24121498..24129962hg38UCSC Ensembl
chr3:24163090..24171318hg19UCSC Ensembl
Innerchr3:24163090..24171318hg19UCSC Ensembl
Outerchr3:24162989..24171453hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg388229
hg198229
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10949571, essv10949572
SamplesHG00142, HG02970
Known GenesTHRB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595571
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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