A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14245262



Internal ID21308372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:99393381..99544016hg38UCSC Ensembl
Outerchr4:99387827..99545452hg38UCSC Ensembl
Innerchr4:100314538..100465173hg19UCSC Ensembl
Outerchr4:100308984..100466609hg19UCSC Ensembl
Innerchr4:100533561..100684196hg18UCSC Ensembl
Outerchr4:100528007..100685632hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38157626
hg19157626
hg18157626
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169903
Supporting Variants
SamplesNGO_41
Known GenesADH7, C4orf17
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14245262
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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