A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14246908



Internal ID21306009
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169825
Supporting Variants
SamplesNGO_24
Known GenesPALLD
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14246908
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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