A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010390



Internal ID18752921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:231576811..231680718hg38UCSC Ensembl
Innerchr1:231712557..231816464hg19UCSC Ensembl
Innerchr1:229779180..229883087hg18UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38103908
hg19103908
hg18103908
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv582n100
Supporting Variantsnssv3705527
Samples
Known GenesDISC1, LINC00582, TSNAX-DISC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010390
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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