A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595253



Internal ID6982571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9860523..9864755hg38UCSC Ensembl
Innerchr3:9860544..9864734hg38UCSC Ensembl
Outerchr3:9860502..9864776hg38UCSC Ensembl
chr3:9902207..9906439hg19UCSC Ensembl
Innerchr3:9902228..9906418hg19UCSC Ensembl
Outerchr3:9902186..9906460hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg384233
hg194233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10918304, essv10918305, essv10918306
SamplesHG03857, NA19443, NA19436
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595253
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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