A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154638



Internal ID22085143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:85578668..85594141hg38UCSC Ensembl
Outerchr10:85575450..85599298hg38UCSC Ensembl
Innerchr10:87338425..87353898hg19UCSC Ensembl
Outerchr10:87335207..87359055hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3823849
hg1923849
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4006061
Samples
Known GenesGRID1-AS1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154638
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer