A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646290



Internal ID7033035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62429901..62472599hg38UCSC Ensembl
Innerchr20:62430401..62472099hg38UCSC Ensembl
Outerchr20:62428901..62473599hg38UCSC Ensembl
chr20:61004957..61047655hg19UCSC Ensembl
Innerchr20:61005457..61047155hg19UCSC Ensembl
Outerchr20:61003957..61048655hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3842699
hg1942699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16221009
SamplesHG01798
Known GenesGATA5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646290
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