A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972813



Internal ID18608029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:138198294..138231177hg38UCSC Ensembl
Innerchr9:141088744..141121627hg19UCSC Ensembl
Innerchr9:140208565..140241448hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3832884
hg1932884
hg1832884
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2569883, nssv2569882, nssv2569879, nssv2569886, nssv2569887, nssv2569880, nssv2569881, nssv2569888, nssv2569885, nssv2569884
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM157B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972813
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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