A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006222



Internal ID19095440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:11895928..11912460hg38UCSC Ensembl
Innerchr3:11937402..11953934hg19UCSC Ensembl
Innerchr3:11912402..11928934hg18UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3816533
hg1916533
hg1816533
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4684n100
Supporting Variantsnssv3591964
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006222
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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