A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13953779



Internal ID6052199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121643289..121650099hg38UCSC Ensembl
Innerchr10:121643289..121650099hg38UCSC Ensembl
Outerchr10:121642789..121650599hg38UCSC Ensembl
chr10:123402803..123409613hg19UCSC Ensembl
Innerchr10:123402803..123409613hg19UCSC Ensembl
Outerchr10:123402303..123410113hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg386811
hg196811
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624754
Supporting Variants
SamplesNA19449
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13953779
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