A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170274



Internal ID21314335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:155763308..155774388hg38UCSC Ensembl
Outerchr3:155758758..155795620hg38UCSC Ensembl
Innerchr3:155481097..155492177hg19UCSC Ensembl
Outerchr3:155476547..155513409hg19UCSC Ensembl
Innerchr3:156963791..156974871hg18UCSC Ensembl
Outerchr3:156959241..156996103hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3836863
hg1936863
hg1836863
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247578
SamplesMLY_9
Known GenesC3orf33
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170274
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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