A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156024



Internal ID22086529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149245607..149250334hg38UCSC Ensembl
Outerchr3:149245205..149253293hg38UCSC Ensembl
Innerchr3:148963394..148968121hg19UCSC Ensembl
Outerchr3:148962992..148971080hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg388089
hg198089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015903, nssv4015900, nssv4015905, nssv4015915, nssv4015904, nssv4015911, nssv4015909, nssv4015918, nssv4015908, nssv4015901, nssv4015916, nssv4015912, nssv4015913, nssv4015917, nssv4015902, nssv4015907, nssv4015914, nssv4015910, nssv4015906
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156024
Frequency
Sample Size131
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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