A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015081



Internal ID19104298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:125816644..125885234hg38UCSC Ensembl
Innerchr4:126737799..126806389hg19UCSC Ensembl
Innerchr4:126957249..127025839hg18UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg3868591
hg1968591
hg1868591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5383n100
Supporting Variantsnssv3743094
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)nsv1015081
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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