A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031363



Internal ID19120585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:178393068..178514706hg38UCSC Ensembl
Innerchr4:179314222..179435860hg19UCSC Ensembl
Innerchr4:179551216..179672854hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38121639
hg19121639
hg18121639
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635552
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)nsv1031363
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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