A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14245198



Internal ID21305918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:29129882..29186909hg38UCSC Ensembl
Outerchr4:29127656..29189135hg38UCSC Ensembl
Innerchr4:29131504..29188531hg19UCSC Ensembl
Outerchr4:29129278..29190757hg19UCSC Ensembl
Innerchr4:28740602..28797629hg18UCSC Ensembl
Outerchr4:28738376..28799855hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3861480
hg1961480
hg1861480
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170094
Supporting Variants
SamplesNGO_24
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14245198
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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