A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039896



Internal ID19129115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:57138666..57200966hg38UCSC Ensembl
Innerchr13:57712800..57775100hg19UCSC Ensembl
Innerchr13:56610801..56673101hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3862301
hg1962301
hg1862301
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1664n100
Supporting Variantsnssv3523917, nssv3523918, nssv3523919, nssv3523916
Samples
Known GenesPRR20A, PRR20B, PRR20C, PRR20D, PRR20E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039896
Frequency
Sample Size11257
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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