A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012425



Internal ID19101642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176177207..176218085hg38UCSC Ensembl
Innerchr3:175894995..175935873hg19UCSC Ensembl
Innerchr3:177377689..177418567hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3840879
hg1940879
hg1840879
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4991n100
Supporting Variantsnssv3614934
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)nsv1012425
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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