A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169584



Internal ID21313817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:91481474..92144389hg38UCSC Ensembl
Outerchr4:91477538..92150014hg38UCSC Ensembl
Innerchr4:92402625..93065540hg19UCSC Ensembl
Outerchr4:92398689..93071165hg19UCSC Ensembl
Innerchr4:92621648..93284563hg18UCSC Ensembl
Outerchr4:92617712..93290188hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38672477
hg19672477
hg18672477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14241508
SamplesMLY_15
Known GenesCCSER1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169584
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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