A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018943



Internal ID19108160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:156520630..156692689hg38UCSC Ensembl
Innerchr4:157441782..157613841hg19UCSC Ensembl
Innerchr4:157661232..157833291hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38172060
hg19172060
hg18172060
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636143
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)nsv1018943
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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