A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008606



Internal ID18751137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:65386381..65500309hg38UCSC Ensembl
Innerchr1:65852064..65965992hg19UCSC Ensembl
Innerchr1:65624652..65738580hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38113929
hg19113929
hg18113929
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv174n100
Supporting Variantsnssv3701244
Samples
Known GenesDNAJC6, LEPR, LEPROT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008606
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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