A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017923



Internal ID19107140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131025220..131433691hg38UCSC Ensembl
Innerchr4:131946375..132354846hg19UCSC Ensembl
Innerchr4:132165825..132574296hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38408472
hg19408472
hg18408472
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5388n100
Supporting Variantsnssv3639460, nssv3639461
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)nsv1017923
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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