A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044331



Internal ID19133550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103261304..103360796hg38UCSC Ensembl
Innerchr13:103913654..104013146hg19UCSC Ensembl
Innerchr13:102711655..102811147hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3899493
hg1999493
hg1899493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713291
Samples
Known GenesMIR548AS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044331
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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