A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169746



Internal ID21313557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:38662929..38670533hg38UCSC Ensembl
Outerchr1:38653411..38671983hg38UCSC Ensembl
Innerchr1:39128601..39136205hg19UCSC Ensembl
Outerchr1:39119083..39137655hg19UCSC Ensembl
Innerchr1:38901188..38908792hg18UCSC Ensembl
Outerchr1:38891670..38910242hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3818573
hg1918573
hg1818573
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245106
SamplesNGO_1
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169746
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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