A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014031



Internal ID19103251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:155763308..155806988hg38UCSC Ensembl
Innerchr3:155481097..155524777hg19UCSC Ensembl
Innerchr3:156963791..157007471hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3843681
hg1943681
hg1843681
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4928n100
Supporting Variantsnssv3606382
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)nsv1014031
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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