A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14248497



Internal ID21301812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149245607..149250334hg38UCSC Ensembl
Outerchr3:149245205..149253293hg38UCSC Ensembl
Innerchr3:148963394..148968121hg19UCSC Ensembl
Outerchr3:148962992..148971080hg19UCSC Ensembl
Innerchr3:150446084..150450811hg18UCSC Ensembl
Outerchr3:150445682..150453770hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg388089
hg198089
hg188089
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169386
Supporting Variants
SamplesMLY_10
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14248497
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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