A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154645



Internal ID22085150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89183210..89191098hg38UCSC Ensembl
Outerchr10:89178916..89194672hg38UCSC Ensembl
Innerchr10:90942967..90950855hg19UCSC Ensembl
Outerchr10:90938673..90954429hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3815757
hg1915757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv40n97
Supporting Variantsnssv4006073, nssv4006074
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154645
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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