A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14251981



Internal ID21311983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68620262..68640616hg38UCSC Ensembl
Outerchr4:68620261..68655691hg38UCSC Ensembl
Innerchr4:69485980..69506334hg19UCSC Ensembl
Outerchr4:69485979..69521409hg19UCSC Ensembl
Innerchr4:69168575..69188929hg18UCSC Ensembl
Outerchr4:69168574..69204004hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3835431
hg1935431
hg1835431
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170256
Supporting Variants
SamplesSNI_14
Known GenesUGT2B15
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14251981
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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