A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154644



Internal ID22085149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89183210..89188333hg38UCSC Ensembl
Outerchr10:89178916..89190337hg38UCSC Ensembl
Innerchr10:90942967..90948090hg19UCSC Ensembl
Outerchr10:90938673..90950094hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3811422
hg1911422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv40n97
Supporting Variantsnssv4006072, nssv4006070, nssv4006071
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154644
Frequency
Sample Size131
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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