A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169776



Internal ID21313587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:36864410..36919169hg38UCSC Ensembl
Outerchr3:36863292..36924539hg38UCSC Ensembl
Innerchr3:36905901..36960660hg19UCSC Ensembl
Outerchr3:36904783..36966030hg19UCSC Ensembl
Innerchr3:36880905..36935664hg18UCSC Ensembl
Outerchr3:36879787..36941034hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3861248
hg1961248
hg1861248
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14251335
SamplesPML_1
Known GenesTRANK1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169776
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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