A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999641



Internal ID19159177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:155763308..155816827hg38UCSC Ensembl
Innerchr3:155481097..155534616hg19UCSC Ensembl
Innerchr3:156963791..157017310hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3853520
hg1953520
hg1853520
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4928n100
Supporting Variantsnssv3606383
Samples
Known GenesC3orf33
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999641
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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