A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14245113



Internal ID21306871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:99399959..99556305hg38UCSC Ensembl
Outerchr4:99393381..99561532hg38UCSC Ensembl
Innerchr4:100321116..100477462hg19UCSC Ensembl
Outerchr4:100314538..100482689hg19UCSC Ensembl
Innerchr4:100540139..100696485hg18UCSC Ensembl
Outerchr4:100533561..100701712hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38168152
hg19168152
hg18168152
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169903
Supporting Variants
SamplesNGO_30
Known GenesADH7, C4orf17, TRMT10A
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14245113
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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