A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14250335



Internal ID21305747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:107144594..107147256hg38UCSC Ensembl
Outerchr4:107130343..107150362hg38UCSC Ensembl
Innerchr4:108065751..108068413hg19UCSC Ensembl
Outerchr4:108051500..108071519hg19UCSC Ensembl
Innerchr4:108285200..108287862hg18UCSC Ensembl
Outerchr4:108270949..108290968hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3820020
hg1920020
hg1820020
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170210
Supporting Variants
SamplesNGO_23
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14250335
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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