A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026698



Internal ID19115916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131025220..131440539hg38UCSC Ensembl
Innerchr4:131946375..132361694hg19UCSC Ensembl
Innerchr4:132165825..132581144hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38415320
hg19415320
hg18415320
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5388n100
Supporting Variantsnssv3743106, nssv3743107
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)nsv1026698
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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