A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983615



Internal ID18618808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:94758581..94761036hg38UCSC Ensembl
Innerchr13:95410835..95413290hg19UCSC Ensembl
Innerchr13:94208836..94211291hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg382456
hg192456
hg182456
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1972014, nssv1972016, nssv1972018, nssv1972017, nssv1972011, nssv1972010, nssv1972019, nssv1972013, nssv1972012, nssv1972015
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)nsv983615
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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