A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13861918



Internal ID6317934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73606004..73608789hg38UCSC Ensembl
Innerchr10:73606043..73608751hg38UCSC Ensembl
Outerchr10:73605966..73608828hg38UCSC Ensembl
chr10:75365762..75368547hg19UCSC Ensembl
Innerchr10:75365801..75368509hg19UCSC Ensembl
Outerchr10:75365724..75368586hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg382786
hg192786
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623816
Supporting Variants
SamplesNA19917
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13861918
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