A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14252177



Internal ID21308756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:99393381..99545854hg38UCSC Ensembl
Outerchr4:99387827..99546452hg38UCSC Ensembl
Innerchr4:100314538..100467011hg19UCSC Ensembl
Outerchr4:100308984..100467609hg19UCSC Ensembl
Innerchr4:100533561..100686034hg18UCSC Ensembl
Outerchr4:100528007..100686632hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38158626
hg19158626
hg18158626
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169903
Supporting Variants
SamplesNGO_44
Known GenesADH7, C4orf17
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14252177
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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