A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169404



Internal ID21313887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3375059..3447474hg38UCSC Ensembl
Outerchr1:3371973..3449184hg38UCSC Ensembl
Innerchr1:3291623..3364038hg19UCSC Ensembl
Outerchr1:3288537..3365748hg19UCSC Ensembl
Innerchr1:3281483..3353898hg18UCSC Ensembl
Outerchr1:3278397..3355608hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3877212
hg1977212
hg1877212
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14248196
SamplesNGO_23
Known GenesPRDM16
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169404
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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