A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169825



Internal ID21313636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:168802571..168838853hg38UCSC Ensembl
Outerchr4:168802179..168841303hg38UCSC Ensembl
Innerchr4:169723722..169760004hg19UCSC Ensembl
Outerchr4:169723330..169762454hg19UCSC Ensembl
Innerchr4:169960297..169996579hg18UCSC Ensembl
Outerchr4:169959905..169999029hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3839125
hg1939125
hg1839125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14248469, nssv14251391, nssv14242750, nssv14246908
SamplesNGO_43, NGO_24, NGO_19, NGO_33
Known GenesPALLD
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169825
Frequency
Sample Size93
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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