A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623765



Internal ID6663932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70436517..70438256hg38UCSC Ensembl
Innerchr10:70436519..70438254hg38UCSC Ensembl
Outerchr10:70436515..70438258hg38UCSC Ensembl
chr10:72196273..72198012hg19UCSC Ensembl
Innerchr10:72196275..72198010hg19UCSC Ensembl
Outerchr10:72196271..72198014hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381740
hg191740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13858618
SamplesHG01783
Known GenesNODAL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623765
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