A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3743106



Internal ID19041387
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 StatusS
Merged Variantsnsv1026698
Supporting Variants
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)nssv3743106
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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