A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169948



Internal ID21314009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:82919029..82979908hg38UCSC Ensembl
Outerchr13:82912861..82982433hg38UCSC Ensembl
Innerchr13:83493164..83554043hg19UCSC Ensembl
Outerchr13:83486996..83556568hg19UCSC Ensembl
Innerchr13:82391165..82452044hg18UCSC Ensembl
Outerchr13:82384997..82454569hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3869573
hg1969573
hg1869573
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249650
SamplesPML_1
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169948
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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