A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044601



Internal ID19133820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:102040178..102077962hg38UCSC Ensembl
Innerchr13:102692528..102730312hg19UCSC Ensembl
Innerchr13:101490529..101528313hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3837785
hg1937785
hg1837785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525533
Samples
Known GenesFGF14, MIR4705
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044601
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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