A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030454



Internal ID19119673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161099011..161174743hg38UCSC Ensembl
Innerchr4:162020163..162095895hg19UCSC Ensembl
Innerchr4:162239613..162315345hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3875733
hg1975733
hg1875733
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3634142
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)nsv1030454
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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