A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013200



Internal ID19102418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:168363492..168388521hg38UCSC Ensembl
Innerchr1:168332730..168357759hg19UCSC Ensembl
Innerchr1:166599354..166624383hg18UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3825030
hg1925030
hg1825030
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3496951
Samples
Known GenesMIR557
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013200
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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