A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169711



Internal ID21313522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:102096726..102102622hg38UCSC Ensembl
Outerchr1:102092229..102109708hg38UCSC Ensembl
Innerchr1:102562282..102568178hg19UCSC Ensembl
Outerchr1:102557785..102575264hg19UCSC Ensembl
Innerchr1:102334870..102340766hg18UCSC Ensembl
Outerchr1:102330373..102347852hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3817480
hg1917480
hg1817480
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249255
SamplesNGO_24
Known GenesMIR548AI
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169711
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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