A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039844



Internal ID19129063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19089259..19160695hg38UCSC Ensembl
Innerchr13:19663399..19734835hg19UCSC Ensembl
Innerchr13:18561399..18632835hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3871437
hg1971437
hg1871437
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3714936
Samples
Known GenesRNU6-52P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039844
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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