A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000569



Internal ID18743100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:159992675..160017285hg38UCSC Ensembl
Innerchr1:159962465..159987075hg19UCSC Ensembl
Innerchr1:158229089..158253699hg18UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3824611
hg1924611
hg1824611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv446n100
Supporting Variantsnssv3500651
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)nsv1000569
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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