A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044644



Internal ID19133863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112437023..113055517hg38UCSC Ensembl
Innerchr13:113091337..113709831hg19UCSC Ensembl
Innerchr13:112139338..112757832hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38618495
hg19618495
hg18618495
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713323
Samples
Known GenesATP11A, C13orf35, MCF2L, MCF2L-AS1, TUBGCP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044644
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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