A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13764219



Internal ID5322860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42888799..42892128hg38UCSC Ensembl
Innerchr10:42888826..42892102hg38UCSC Ensembl
Outerchr10:42888773..42892155hg38UCSC Ensembl
chr10:43384247..43387576hg19UCSC Ensembl
Innerchr10:43384274..43387550hg19UCSC Ensembl
Outerchr10:43384221..43387603hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg383330
hg193330
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623032
Supporting Variants
SamplesNA18867
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13764219
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