A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032841



Internal ID19122063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:135774638..135852547hg38UCSC Ensembl
Innerchr5:135110327..135188236hg19UCSC Ensembl
Innerchr5:135138226..135216135hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3877910
hg1977910
hg1877910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648127
Samples
Known GenesSLC25A48
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032841
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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