A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154434



Internal ID22084939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:179361393..179364180hg38UCSC Ensembl
Outerchr1:179354603..179370071hg38UCSC Ensembl
Innerchr1:179330528..179333315hg19UCSC Ensembl
Outerchr1:179323738..179339206hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3815469
hg1915469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005215, nssv4005214, nssv4005212, nssv4005218, nssv4005213, nssv4005211, nssv4005217, nssv4005216
Samples
Known GenesAXDND1, SOAT1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154434
Frequency
Sample Size131
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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