A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983618



Internal ID18618811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:104814313..104816576hg38UCSC Ensembl
Innerchr13:105466664..105468927hg19UCSC Ensembl
Innerchr13:104264665..104266928hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg382264
hg192264
hg182264
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1974795, nssv1974789, nssv1974792, nssv1974786, nssv1974791, nssv1974793, nssv1974788, nssv1974794, nssv1974787, nssv1974790
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983618
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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