A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169608



Internal ID21313841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:105491310..105713804hg38UCSC Ensembl
Outerchr1:105487979..105726548hg38UCSC Ensembl
Innerchr1:106033932..106256426hg19UCSC Ensembl
Outerchr1:106030601..106269170hg19UCSC Ensembl
Innerchr1:105835455..106057949hg18UCSC Ensembl
Outerchr1:105832124..106070693hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38238570
hg19238570
hg18238570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14250475, nssv14250583, nssv14247932, nssv14244064
SamplesMLY_1, PML_1, MLY_2, MLY_14
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169608
Frequency
Sample Size93
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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