A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247578



Internal ID21303779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:155763307..155774388hg38UCSC Ensembl
Outerchr3:155758758..155795620hg38UCSC Ensembl
Innerchr3:155481096..155492177hg19UCSC Ensembl
Outerchr3:155476547..155513409hg19UCSC Ensembl
Innerchr3:156963790..156974871hg18UCSC Ensembl
Outerchr3:156959241..156996103hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3836863
hg1936863
hg1836863
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170274
Supporting Variants
SamplesMLY_9
Known GenesC3orf33
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247578
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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