A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169386



Internal ID21313869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149245608..149250334hg38UCSC Ensembl
Outerchr3:149245205..149253293hg38UCSC Ensembl
Innerchr3:148963395..148968121hg19UCSC Ensembl
Outerchr3:148962992..148971080hg19UCSC Ensembl
Innerchr3:150446085..150450811hg18UCSC Ensembl
Outerchr3:150445682..150453770hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg388089
hg198089
hg188089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245078, nssv14249553, nssv14241883, nssv14245322, nssv14245386, nssv14248497
SamplesMLY_15, NGO_3, MLY_11, NGO_2, MLY_10, SNI_4
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169386
Frequency
Sample Size93
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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