A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006153



Internal ID18748684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:180157901..180202226hg38UCSC Ensembl
Innerchr1:180127036..180171361hg19UCSC Ensembl
Innerchr1:178393659..178437984hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3844326
hg1944326
hg1844326
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv475n100
Supporting Variantsnssv3497274, nssv3484133
Samples
Known GenesFLJ23867, QSOX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006153
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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