A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044793



Internal ID19134012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68932575..69016461hg38UCSC Ensembl
Innerchr13:69506707..69590593hg19UCSC Ensembl
Innerchr13:68404708..68488594hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3883887
hg1983887
hg1883887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3529283
Samples
Known GenesMIR548H4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044793
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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