A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624476



Internal ID7011329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:106664294..106666124hg38UCSC Ensembl
Innerchr10:106664316..106666103hg38UCSC Ensembl
Outerchr10:106664273..106666146hg38UCSC Ensembl
chr10:108424052..108425882hg19UCSC Ensembl
Innerchr10:108424074..108425861hg19UCSC Ensembl
Outerchr10:108424031..108425904hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg381831
hg191831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13927816, essv13927815
SamplesNA18864, HG02557
Known GenesSORCS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624476
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